Liver Cirrhosis, Experimental
|
Prostatic Neoplasms
|
Breast Carcinoma
|
Stomach Neoplasms
|
Autism
|
Hepatocellular Carcinoma
|
Colorectal Cancer
|
Hypertension
|
Obesity
|
Craniofacial Abnormalities
|
Melanoma
|
Endometriosis
|
Lung Neoplasms
|
Diabetes Mellitus, Experimental
|
Neoplasm Invasiveness
|
Colonic Neoplasm
|
Urinary Bladder Neoplasms
|
Mammary Neoplasms, Experimental
|
Drug-Induced Liver Injury
|
Myocardial Ischemia
|
Diabetes Mellitus, Type 2
|
Carcinoma
|
Neoplasm Metastasis
|
Heart Failure
|
Adenocarcinoma
|
Schizophrenia
|
Rheumatoid Arthritis
|
Liver Neoplasms
|
Leukemia, Myeloid, Acute
|
Disease Progression
|
Mammary Neoplasms, Animal
|
Intellectual Disability
|
Inflammation
|
Polycystic Ovary Syndrome
|
Seizures
|
Kidney Disease
|
Esophageal Neoplasms
|
Cell Transformation, Neoplastic
|
Weight Gain
|
Arthritis, Juvenile
|
Ovarian Neoplasms
|
Renal Cell Carcinoma
|
Nerve Degeneration
|
Cardiac Hypertrophy
|
Carcinoma, Adenoid Cystic
|
Squamous Cell Carcinoma
|
Mesothelioma, Malignant
|
Abortion, Spontaneous
|
Myocardial Infarction
|
Glioma
|
Precancerous Conditions
|
Pancreatic Carcinoma
|
Osteoarthritis
|
Carcinoma, Non-Small-Cell Lung
|
Fatty Liver
|
Reperfusion Injury
|
Asthma
|
Liver Cirrhosis
|
Esophageal Squamous Cell Carcinoma
|
Drug Dependence
|
Hyperalgesia
|
Amphetamine-Related Disorders
|
Cardiomyopathies
|
Osteoporosis
|
Liver Neoplasms, Experimental
|
Liver Diseases
|
Atherosclerosis
|
Disease Models, Animal
|
Cholestasis
|
Neoplasms
|
Coronary Artery Disease
|
Insulin Resistance
|
Leukemia, Promyelocytic, Acute
|
Endometrial Neoplasm
|
Male Infertility
|
Psoriasis
|
Systemic Lupus Erythematosus
|
Alzheimer's Disease
|
Glioblastoma Multiforme
|
Parkinson's Disease
|
Neuroblastoma
|
Heart Diseases
|
Brain Ischemia
|
Medulloblastoma
|
Dermatitis, Contact
|
Calcinosis
|
Hiv Infections
|
Neoplasm Recurrence, Local
|
Cocaine Dependence
|
Skin Diseases
|
Skin Neoplasms
|
Anoxia
|
Infertility, Female
|
Influenza, Human
|
Fibrosis
|
Leukemia
|
Diabetes Mellitus
|
Lung Adenocarcinoma
|
Mouth Neoplasms
|
Respiratory Distress Syndrome, Adult
|
Autoimmune Disease
|
Status Epilepticus
|
Autism Spectrum Disorder
|
Myocardial Reperfusion Injury
|
Brain Injuries
|
Necrosis
|
Neurodegenerative Diseases
|
Kidney Failure, Chronic
|
Drug-Related Side Effects And Adverse Reactions
|
Ulcerative Colitis
|
Diabetic Nephropathy
|
Substance Withdrawal Syndrome
|
Pulmonary Hypertension
|
Acute Lymphoblastic Leukemia
|
Ischemia
|
Carcinoma, Transitional Cell
|
Cholangiocarcinoma
|
Hepatolenticular Degeneration
|
Osteosarcoma
|
Astrocytoma
|
Arsenic Poisoning
|
Stroke
|
Unipolar Depression
|
Adenoma
|
Cardiovascular Disease
|
Sezary Syndrome
|
Acute Kidney Injury
|
Non-Alcoholic Fatty Liver Disease
|
Amyotrophic Lateral Sclerosis
|
Mesothelioma
|
Leukemia-Lymphoma, Adult T-Cell
|
Thrombosis
|
Bipolar Disorder
|
Hernia, Diaphragmatic
|
Brain Diseases
|
Growth Disorders
|
Keloid
|
Cardiomyopathy, Hypertrophic
|
Parkinsonian Disorders
|
Arthritis, Experimental
|
Chronic Lymphocytic Leukemia
|
Toxic Epidermal Necrolysis
|
Small Cell Lung Carcinoma
|
Pulmonary Fibrosis
|
Chronic Obstructive Pulmonary Disease
|
Learning Disorders
|
Intracerebral Hemorrhage
|
Kidney Neoplasms
|
Diabetes Mellitus, Type 1
|
Colitis
|
Heart Valve Diseases
|
Hepatitis, Chronic
|
Micronuclei, Chromosome-Defective
|
Cognitive Impairment
|
Ovarian Cysts
|
Oral Submucous Fibrosis
|
Nervous System Diseases
|
Dilated Cardiomyopathy
|
Neoplasms, Experimental
|
Amyotrophic Lateral Sclerosis 1
|
Muscular Diseases
|
Acute Coronary Syndrome
|
Major Depression
|
Cone-Rod Dystrophy 2
|
Anxiety Disorder
|
Thyroid Carcinoma
|
Recurrence
|
Alcoholic Liver Cirrhosis
|
Lymphoma, T-Cell, Cutaneous
|
Peripheral Neuropathy
|
Alcohol Dependence
|
Lung Diseases
|
Marfan Syndrome
|
Memory Disorders
|
Attention Deficit Hyperactivity Disorder
|
Hepatitis
|
Carcinoma, Squamous Cell Of Head And Neck
|
Brain Neoplasms
|
Epilepsy
|
Prostatic Intraepithelial Neoplasia
|
Proteinuria
|
Salivary Gland Neoplasm
|
Basal Cell Carcinoma
|
Lymphoma, Non-Hodgkin
|
Hypotension
|
Left Ventricular Hypertrophy
|
Occupational Diseases
|
Thrombocytopenia
|
Hyperplasia
|
Hypercholesterolemia
|
Bone Diseases, Metabolic
|
Hepatomegaly
|
Pancreatitis
|
Stomach Ulcer
|
Chloracne
|
Chronic Myelogenous Leukemia
|
Heart Defects, Congenital
|
Iga Glomerulonephritis
|
Female Urogenital Diseases
|
Ventricular Dysfunction, Left
|
Enterocolitis, Necrotizing
|
Prenatal Injuries
|
Lymphoma
|
Psychoses, Substance-Induced
|
Adrenocortical Carcinoma
|
Metabolic Syndrome X
|
Retinal Diseases
|
Adenomatous Polyposis Coli
|
Lung Injury
|
Crohn's Disease
|
Acute Lung Injury
|
Lymphoma, T-Cell
|
Liver Diseases, Parasitic
|
Uterine Cervical Neoplasms
|
Myelodysplastic Syndromes
|
Cleft Lip
|
Methylmalonic Acidemia
|
Leukemia, Myelomonocytic, Juvenile
|
Cardiac Arrhythmia
|
Gliosis
|
Albuminuria
|
Pheochromocytoma
|
Pneumonia
|
Precursor T-Cell Lymphoblastic Leukemia-Lymphoma
|
Aortic Diseases
|
Intestinal Neoplasms
|
Eye Abnormalities
|
Preeclampsia
|
Premature Birth
|
Lymphoma, Follicular
|
Infarction, Middle Cerebral Artery
|
Multiple Myeloma
|
Turner Syndrome
|
Limb Dystonia
|
Lymphoma, Large B-Cell, Diffuse
|
Barrett's Esophagus
|
Neural Tube Defects
|
Hypertension, Essential
|
Sepsis
|
Mitochondrial Diseases
|
Idiopathic Pulmonary Fibrosis
|
Allergy
|
Metabolic Diseases
|
Hyperkinesis
|
Hyperglycemia
|
Diabetic Angiopathies
|
Testicular Germ Cell Tumor
|
Language Development Disorders
|
Mitochondrial Complex I Deficiency
|
Pain
|
Mental Retardation, X-Linked
|
Migraine Disorder
|
Retinal Degeneration
|
Bone Neoplasms
|
Ataxia
|
Vascular Diseases
|
Mouth Diseases
|
Hemangiosarcoma
|
Muscular Atrophy
|
Androgenetic Alopecia
|
Tongue Neoplasms
|
Dermatitis, Allergic Contact
|
Leukemia, Myeloid
|
Manganese Poisoning
|
Brain Edema
|
Dermatitis
|
Paralysis
|
Adenocarcinoma Of Esophagus
|
Aicardi-Goutieres Syndrome
|
Aneurysm, Dissecting
|
Aortic Valve Insufficiency
|
Psoriatic Arthritis
|
Asphyxia Neonatorum
|
Asthma, Occupational
|
Atrial Fibrillation
|
Behcet's Syndrome
|
Birth Weight
|
Body Weight
|
Bone Diseases, Developmental
|
Carcinoma, Ductal, Breast
|
Carcinoma, Pancreatic Ductal
|
Cataract
|
Cholangitis
|
Congenital Abnormalities
|
Dementia
|
Developmental Disabilities
|
Gestational Diabetes
|
Diabetic Neuropathies
|
Diabetic Retinopathy
|
Down Syndrome
|
Drug Eruptions
|
Drug Hypersensitivity
|
Duodenal Ulcer
|
Edema
|
Endotoxemia
|
Fever
|
Genetic Predisposition To Disease
|
Glomerulonephritis
|
Focal Segmental Glomerulosclerosis
|
Glucose Intolerance
|
Hearing Loss, Sensorineural
|
Hyperaldosteronism
|
Hyperemia
|
Hyperthyroidism
|
Lead Poisoning
|
Leukemia, Lymphoid
|
Limb Deformities, Congenital
|
Primary Biliary Cirrhosis
|
Lymphoma, T-Cell, Peripheral
|
Age-Related Macular Degeneration
|
Mental Disorders
|
Neointima
|
Nephrotic Syndrome
|
Neurotoxicity Syndromes
|
Osteitis Deformans
|
Osteochondrodysplasias
|
Parkinson Disease, Secondary
|
Pulmonary Emphysema
|
Renal Insufficiency
|
Sjogren Syndrome
|
Skin Abnormalities
|
Spinocerebellar Ataxias
|
Splenomegaly
|
Uremia
|
Uveitis
|
Vasospasm, Intracranial
|
Venous Thrombosis
|
Weight Loss
|
Wounds And Injuries
|
Thromboembolism
|
Oligodendroglioma
|
Meningioma
|
Epilepsy, Absence
|
Muscular Dystrophy, Facioscapulohumeral
|
Muscle Weakness
|
Hearing Loss
|
Hyperparathyroidism, Secondary
|
Cachexia
|
Neurologic Manifestations
|
Respiratory Tract Diseases
|
Thyroid Cancer, Papillary
|
Glaucoma 1, Open Angle, A
|
Atopic Eczema
|
Ischemic Attack, Transient
|
Dyskinesia, Drug-Induced
|
Nasopharyngeal Carcinoma
|
Familial Primary Pulmonary Hypertension
|
Musculoskeletal Pain
|
Immunoblastic Lymphadenopathy
|
Fanconi Anemia
|
Encephalomyelitis, Autoimmune, Experimental
|
Sciatic Neuropathy
|
Peroxisome Biogenesis Disorders
|
Zellweger Syndrome
|
Immunologic Deficiency Syndromes
|
Systemic Scleroderma
|
Burns
|
Lewy Body Dementia
|
Deficiency Diseases
|
Hemolysis
|
Metabolism, Inborn Errors
|
Dyslipidemias
|
Listeriosis
|
Osteogenesis Imperfecta
|
Keratosis
|
Kidney Stone
|
Hematologic Diseases
|
Fatty Liver, Alcoholic
|
Dystonic Disorders
|
Radiation Injuries, Experimental
|
Ehlers-Danlos Syndrome Type 1
|
Hernias, Diaphragmatic, Congenital
|
Muscular Dystrophy-Dystroglycanopathy (Limb-Girdle), Type C, 1
|
Nephrosis
|
Burkitt Lymphoma
|
Demyelinating Diseases
|
Csnb1c
|
Pilomatrixoma
|
Amino Acid Metabolism, Inborn Errors
|
Urticaria
|
Coronary Heart Disease
|
Leukemia, T-Cell
|
Liver Failure, Acute
|
Microsatellite Instability
|
Amenorrhea
|
Pulmonary Embolism
|
Hyperexplexia Hereditary
|
Blood Coagulation Disorders
|
Cardiomyopathy, Hypertrophic, Familial
|
Noonan Syndrome
|
Mitochondrial Encephalomyopathies
|
Furlong Syndrome
|
Pneumoconiosis
|
Brachydactyly
|
Ovarian Epithelial Cancer
|
Carney-Stratakis Syndrome
|
Vascular System Injuries
|
Abnormalities, Multiple
|
Myoclonic Epilepsies, Progressive
|
Silicosis
|
Hypoglycemia
|
Adrenal Hyperplasia, Congenital
|
Primary Ovarian Insufficiency
|
Anemia
|
Hyperinsulinism
|
Celiac Disease
|
Fetal Growth Retardation
|
Endomyocardial Fibrosis
|
Hepatitis C
|
Amnesia
|
Pancreatitis, Chronic
|
Morphine Dependence
|
Ventricular Remodeling
|
Hyperlipidemias
|
Aortic Rupture
|
Cerebral Infarction
|
Movement Disorder
|
Papilloma
|
Hypogonadism
|
Leukoencephalopathies
|
Chromosome Breakage
|
Deafness
|
Leigh Disease
|
Muscle Hypotonia
|
Thoracic Aortic Aneurysm
|
Lymphatic Metastasis
|
Ichthyosiform Erythroderma, Brocq Congenital, Nonbullous Form
|
Adrenal Gland Neoplasms
|
Lipidoses
|
Aortic Aneurysm
|
Ichthyosis, Lamellar
|
Exostoses, Multiple Hereditary
|
Spinal Cord Diseases
|
Carcinoma, Small Cell
|
Organophosphate Poisoning
|
Glaucoma, Angle-Closure
|
Eye Diseases, Hereditary
|
Glaucoma, Primary Open Angle
|
Heredodegenerative Disorders, Nervous System
|
Malaria
|
Ankylosing Spondylitis
|
Alternating Hemiplegia Of Childhood
|
Cryptorchidism
|
Malnutrition
|
Osteogenesis Imperfecta, Type 2a
|
Osteogenesis Imperfecta, Type 3
|
Osteogenesis Imperfecta, Type 4
|
Apraxias
|
Mandibular Diseases
|
Infection
|
Heterotaxy Syndrome
|
Chondroma
|
Basal Ganglia Diseases
|
Inflammatory Bowel Disease
|
Brain Infarction
|
Glomerulonephritis, Membranoproliferative
|
Abruptio Placentae
|
Bone Diseases
|
Bartter Syndrome, Type 4a
|
Mastocytosis, Systemic
|
Intervertebral Disc Disease
|
Vitamin A Deficiency
|
Pancreatic Diseases
|
Vitamin D Deficiency
|
Tachycardia
|
Ehlers-Danlos Syndrome, Type Vii, Autosomal Dominant
|
Tachycardia, Ventricular
|
Intestinal Perforation
|
Paraganglioma
|
Megaepiphyseal Dwarfism
|
Paranoid Disorders
|
Melanoma, Experimental
|
Thrombocythemia, Essential
|
Paratuberculosis
|
Melas Syndrome
|
Thrombocytosis
|
Thrombophilia
|
Intestinal Polyps
|
Venous Thromboembolism
|
Iron Metabolism Disorders
|
Meningomyelocele
|
Pasteurellaceae Infections
|
Thymoma
|
Menkes Kinky Hair Syndrome
|
Iron Overload
|
Coronary Restenosis
|
Thyroid Diseases
|
Emphysema
|
Combined Cellular And Humoral Immune Defects With Granulomas
|
Jaw Abnormalities
|
Periodontitis
|
Peritoneal Neoplasms
|
Hydronephrosis
|
Enchondromatosis
|
Juvenile Polyposis Syndrome
|
Angioedema
|
Granulomatous Disease, Chronic
|
Bardet-Biedl Syndrome
|
Endocrine System Diseases
|
Trigeminal Neuralgia
|
Tuberculosis, Pulmonary
|
Tyrosinemias
|
Ureteral Calculi
|
Hypercalcemia
|
Phyllodes Tumor
|
Urinary Bladder Diseases
|
Piebaldism
|
46, Xy Disorders Of Sex Development
|
Kidney Tubular Necrosis, Acute
|
Graves Ophthalmopathy
|
Microcephaly
|
Budd-Chiari Syndrome
|
Deafness, Autosomal Recessive 12
|
Fetal Alcohol Spectrum Disorders
|
Anemia, Sideroblastic
|
Migraine Without Aura
|
Kyphosis
|
Cardiovascular Abnormalities
|
Hyperhomocysteinemia
|
Growth Hormone-Secreting Pituitary Adenoma
|
Carotid Artery Diseases
|
Pneumonia, Pneumococcal
|
Mitral Valve Insufficiency
|
Cartilage Diseases
|
Catalepsy
|
Uveal Melanoma
|
Poisoning
|
Polycystic Kidney, Autosomal Dominant
|
Polycythemia
|
Molybdenum Cofactor Deficiency
|
Mood Disorder
|
Hyperlipoproteinemias
|
Hypercholesterolemia, Familial
|
Ceroid Lipofuscinosis, Neuronal 1, Infantile
|
Leber Congenital Amaurosis
|
Mucopolysaccharidosis Iii
|
Duane Retraction Syndrome
|
Uterine Fibroid
|
Leiomyosarcoma
|
Leishmaniasis
|
Chilblain Lupus 1
|
Breast Neoplasms, Male
|
Multiple Organ Failure
|
Xeroderma Pigmentosum
|
Visceral Leishmaniasis
|
Multiple Sclerosis
|
Precursor B-Cell Lymphoblastic Leukemia-Lymphoma
|
Muscle Rigidity
|
Anemia, Hemolytic
|
Ductus Arteriosus, Patent
|
Aging, Premature
|
Coronary Vasospasm
|
Costello Syndrome
|
Cardiomyopathy, Dilated, 3b
|
Progeria
|
Foot Deformities, Congenital
|
Head And Neck Neoplasms
|
Myasthenic Syndrome, Congenital, Type Id
|
Prostate Cancer, Familial
|
Mycoplasma Infections
|
Fractures, Bone
|
Myeloproliferative Disorder
|
Afibrinogenemia
|
Protein Deficiency
|
Chondrosarcoma
|
Diabetes Mellitus, Transient Neonatal, 1
|
Pseudohypoaldosteronism
|
Myocardial Stunning
|
Bradycardia
|
Adrenoleukodystrophy
|
Leukemia, Megakaryoblastic, Of Down Syndrome
|
Leukemia, Monocytic, Acute
|
Atypical Hemolytic Uremic Syndrome
|
Psychosis
|
Puberty, Precocious
|
Adrenal Insufficiency
|
Pulmonary Edema
|
Nephroblastoma
|
Fraser Syndrome
|
Colonic Polyps
|
Myopia
|
Cowden-Like Syndrome
|
Myotonia
|
Myotonic Dystrophy
|
Atrophy
|
Nasopharyngeal Neoplasm
|
Epilepsy, Temporal Lobe
|
Hemangioma
|
Hypertriglyceridemia
|
Hypertrophy
|
Neoplasms, Germ Cell And Embryonal
|
Chondrosarcoma, Extraskeletal Myxoid
|
Neoplasms, Second Primary
|
Respiratory Hypersensitivity
|
Neoplasms, Squamous Cell
|
Neovascularization, Pathologic
|
Reticuloendotheliosis, Familial, With Eosinophilia
|
Nephritis, Interstitial
|
Li-Fraumeni Syndrome
|
Retinal Vein Occlusion
|
Nerve Sheath Neoplasms
|
Nervous System Malformations
|
Neuropathic Pain
|
Amelogenesis Imperfecta, Hypomaturation Type, Iia1
|
Neurilemmoma
|
Rickets
|
Neurobehavioral Manifestations
|
Copper-Overload Cirrhosis
|
Rubinstein-Taybi Syndrome
|
Neuroectodermal Tumors, Primitive
|
Neuroendocrine Tumors
|
Gastroesophageal Reflux
|
Neurogenic Inflammation
|
Sarcoma
|
Ewing Sarcoma
|
Neuronal Ceroid-Lipofuscinoses
|
Schistosomiasis
|
Schistosomiasis Mansoni
|
Lipodystrophy
|
Gastrointestinal Diseases
|
Scrapie
|
Cardiofaciocutaneous Syndrome
|
Hemophilia A
|
Gastrointestinal Stromal Tumors
|
Bronchial Hyperreactivity
|
Severe Combined Immunodeficiency, Autosomal Recessive, T Cell-Negative, B Cell-Negative, Nk Cell-Positive
|
Hypopituitarism
|
Aspirin Induced Asthma
|
Gaucher Disease
|
Asbestosis
|
Cholestasis, Intrahepatic
|
Esophagitis
|
Silver-Russell Syndrome
|
Hypothermia
|
Vestibular Diseases
|
Hepatitis B
|
Carcinogenesis
|
Arthritis
|
Acromegaly
|
Skin Ulcer
|
Lupus Nephritis
|
Arteritis
|
Genomic Instability
|
Exfoliation Syndrome
|
Oligospermia
|
Ophthalmoplegia, Chronic Progressive External
|
Beta-Thalassemia
|
Hypertension, Pregnancy-Induced
|
Bifid Nose With Or Without Anorectal And Renal Anomalies
|
Hypertension, Renovascular
|
Vulvar Lichen Sclerosus
|
Hyperthyroxinemia, Familial Dysalbuminemic
|
Bifid Nose
|
Hyperventilation
|
Hypoalbuminemia
|
Hypoaldosteronism
|
Hypogammaglobulinemia And Isolated Growth Hormone Deficiency, X-Linked
|
Hypokalemia
|
Hypokinesia
|
Hypomagnesemia 1, Intestinal
|
Hypomyelination, Global Cerebral
|
Hypophosphatasia, Adult
|
Hypophosphatasia, Childhood
|
Hypophosphatasia, Infantile
|
Hypophosphatemia
|
Hypophosphatemic Rickets, Autosomal Recessive, 2
|
Hypopigmentation
|
Hypospadias
|
Hypospadias 1, X-Linked
|
Beta-Ureidopropionase Deficiency
|
Hypothalamic Hamartomas
|
Hypotonia-Cystinuria Syndrome
|
Hypotrichosis
|
Hypotrichosis And Recurrent Skin Vesicles
|
Hypoxia-Ischemia, Brain
|
Ichthyosis Follicularis Atrichia Photophobia Syndrome
|
Ichthyosis, X-Linked
|
Iga Deficiency
|
Ige Responsiveness, Atopic
|
Ileitis
|
Immune Complex Diseases
|
Immune Dysfunction With T-Cell Inactivation Due To Calcium Entry Defect 2
|
Immune Dysregulation, Polyendocrinopathy, Enteropathy, X-Linked Syndrome
|
Immune System Disease
|
Immunodeficiency Without Anhidrotic Ectodermal Dysplasia
|
Inclusion Body Myopathy Autosomal Recessive
|
Incontinentia Pigmenti
|
Infant, Premature, Diseases
|
Beta Ketothiolase Deficiency
|
Infertility
|
Berylliosis
|
Beckwith-Wiedemann Syndrome
|
Basal Cell Nevus Syndrome
|
Insomnia, Fatal Familial
|
Bartter Syndrome, Type 4b
|
Intervertebral Disc Degeneration
|
Intervertebral Disc Displacement
|
Intestinal Diseases
|
Bartter Syndrome, Type 3
|
Intestinal Polyposis
|
Invasive Pneumococcal Disease, Recurrent Isolated, 2
|
Bartter Syndrome
|
Isolated Growth Hormone Deficiency, Type Ib
|
Isolated Growth Hormone Deficiency, Type Ii
|
Jaundice, Neonatal
|
Johanson Blizzard Syndrome
|
Joint Diseases
|
Joint Instability
|
Juvenile Macular Degeneration And Hypotrichosis
|
Juvenile Polyposis With Hereditary Hemorrhagic Telangiectasia
|
Kabuki Syndrome
|
Keratoacanthoma Familial
|
Barakat Syndrome
|
Balkan Nephropathy
|
Azotemia
|
Kleefstra Syndrome
|
Kniest Dysplasia
|
Knobloch Syndrome
|
Korsakoff Syndrome
|
Kowarski Syndrome
|
Kufor-Rakeb Syndrome
|
Lafora Disease
|
Lameness, Animal
|
Landau-Kleffner Syndrome
|
Langer-Giedion Syndrome
|
Azoospermia
|
Laryngeal Neoplasms
|
Waardenburg Syndrome, Type 2d
|
Lead Poisoning, Nervous System
|
Autonomic Nervous System Diseases
|
Legg-Calve-Perthes Disease
|
Leishmaniasis, Cutaneous
|
Lens Diseases
|
Leopard Syndrome
|
Leopard Syndrome, 2
|
Leprosy
|
Lethargy
|
Autoimmune Polyendocrinopathy Syndrome, Type 1
|
Leukemia, Erythroblastic, Acute
|
Auditory Neuropathy, Autosomal Dominant, 1
|
Wagr Syndrome
|
Atypical Mycobacteriosis, Familial, X-Linked 1
|
Leukemia, Megakaryoblastic, Acute
|
Attention Deficit And Disruptive Behavior Disorders
|
Leukemia, Myeloid, Accelerated Phase
|
Atr-X Syndrome
|
Leukemia, Myelomonocytic, Acute
|
Atrioventricular Block
|
Leukocyte-Adhesion Deficiency Syndrome
|
Leukocyte Adhesion Deficiency Type 1
|
Leukocyte Disorders
|
Leukodystrophy, Metachromatic
|
Leukoplakia, Oral
|
Leukostasis
|
Li-Fraumeni Syndrome 2
|
Lig4 Syndrome
|
Limb-Girdle Muscular Dystrophy Type 2a
|
Limb-Girdle Muscular Dystrophy, Type 2b
|
Limb-Girdle Muscular Dystrophy Type 2h
|
Limb-Mammary Syndrome
|
Lipid Metabolism, Inborn Errors
|
Lipoblastoma
|
Lipodystrophy, Familial Partial
|
Lipoid Congenital Adrenal Hyperplasia
|
Liposarcoma, Myxoid
|
Lithiasis
|
Atrichia With Papular Lesions
|
Atrial Septal Defect 6
|
Wallerian Degeneration
|
Atrial Septal Defect 2
|
Asperger Syndrome
|
Arts Syndrome
|
Long Qt Syndrome
|
Low Back Pain
|
Dyskeratosis Congenita, Autosomal Dominant
|
Interstitial Lung Disease
|
Lung Diseases, Obstructive
|
Dyskeratosis Congenita
|
Dyschromatosis Symmetrica Hereditaria 1
|
Lymphedema
|
Lymphoma, B-Cell
|
Arteriosclerosis
|
Arterial Occlusive Diseases
|
Lymphoma, Mantle-Cell
|
Arterial Calcification Of Infancy
|
Arrhythmogenic Right Ventricular Dysplasia, Familial, 11
|
Arrhythmogenic Right Ventricular Dysplasia, Familial, 10
|
Weaver Syndrome
|
Lymphoproliferative Syndrome, Ebv-Associated, Autosomal, 1
|
Lymphoproliferative Syndrome, X-Linked, 2
|
Macrostomia
|
2-Hydroxyglutaricaciduria
|
Macular Degeneration, Age-Related, 1
|
Macular Degeneration, Age-Related, 4
|
Major Affective Disorder 1
|
Malignant Hyperthermia Susceptibility Type 5
|
Malpuech Facial Clefting Syndrome
|
Aromatase Deficiency
|
Mandibular Neoplasms
|
Mandibuloacral Dysplasia With Type A Lipodystrophy
|
Mandibuloacral Dysplasia With Type B Lipodystrophy
|
Apnea
|
Maple Syrup Urine Disease
|
Aortic Valve, Calcification Of
|
Marie Unna Congenital Hypotrichosis
|
Marles Greenberg Persaud Syndrome
|
Marshall Syndrome
|
Mason-Type Diabetes
|
Masp2 Deficiency
|
Maturity-Onset Diabetes Of The Young, Type 1
|
Maturity-Onset Diabetes Of The Young, Type 7
|
Maxillary Diseases
|
Meacham Syndrome
|
Megacolon
|
Megalocytic Interstitial Nephritis
|
Meningitis
|
Meningitis, Aseptic
|
Meningococcal Infection
|
Xeroderma Pigmentosum, Variant Type
|
Mental Retardation, Autosomal Dominant 3
|
Mental Retardation, Autosomal Recessive 2
|
Mental Retardation-Hypotonic Facies Syndrome, X-Linked, 1
|
Anuria
|
Mental Retardation, X-Linked 30
|
Mental Retardation, X-Linked 45
|
Mental Retardation, X-Linked 63
|
Mental Retardation, X-Linked, Syndromic, Jarid1c-Related
|
Meretoja Syndrome
|
Mesenteric Ischemia
|
Mesenteric Vascular Occlusion
|
Anovulation
|
Angina, Unstable
|
Angina, Stable
|
Metaphyseal Anadysplasia 2
|
Metaphyseal Chondrodysplasia Schmid Type
|
Methemoglobinemia
|
Methemoglobinemia Type Iv
|
Methylcobalamin Deficiency, Cblg Type
|
Angelman Syndrome
|
Methylmalonic Aciduria Due To Methylmalonyl-Coa Mutase Deficiency
|
Methylmalonyl-Coa Epimerase Deficiency
|
Anemia, Sideroblastic, Pyridoxine-Refractory, Autosomal Recessive
|
Microphthalmia, Isolated, With Coloboma 5
|
Microphthalmia, Syndromic 7
|
Mild Cognitive Impairment
|
Sickle Cell Anemia
|
Anemia, Megaloblastic
|
Mitochondrial Myopathies
|
Mitochondrial Neurogastrointestinal Encephalopathy Syndrome
|
Mitral Valve Prolapse
|
Miyoshi Myopathy
|
Jensen Syndrome
|
Motor Neuron Disease
|
Anemia, Iron-Deficiency
|
Anemia, Hypoplastic, Congenital
|
Mowat-Wilson Syndrome
|
Mucopolysaccharidosis Ii
|
Mucopolysaccharidosis Iv
|
Mucopolysaccharidosis Vi
|
Mulibrey Nanism
|
Multiple Acyl Coenzyme A Dehydrogenase Deficiency
|
Multiple Chemical Sensitivity
|
Anemia, Hemolytic, Congenital Nonspherocytic
|
Multiple Sulfatase Deficiency Disease
|
Anemia, Dyserythropoietic, Congenital
|
Muscular Dystrophies
|
Muscular Dystrophy, Animal
|
Muscular Dystrophy, Congenital, Due To Integrin Alpha-7 Deficiency
|
Musculoskeletal Abnormalities
|
Myasthenia Gravis
|
Anemia, Aplastic
|
Myeloperoxidase Deficiency
|
Androgen-Insensitivity Syndrome
|
Anaplasia
|
Myocarditis
|
Myopathy, Distal, With Anterior Tibial Onset
|
Myopathy, Reducing Body, X-Linked, Childhood-Onset
|
Myopathy, Reducing Body, X-Linked, Early-Onset, Severe
|
Myopathy With Lactic Acidosis, Hereditary
|
Myopathy, X-Linked, With Postural Muscle Atrophy
|
Myositis, Inclusion Body
|
Myositis Ossificans
|
Nail-Patella Syndrome
|
Amyotrophic Lateral Sclerosis 6, Autosomal Recessive
|
Weill-Marchesani-Like Syndrome
|
Neonatal-Onset Citrullinemia Type 2
|
Amyloidosis, Familial Visceral
|
Amyloidosis, Familial
|
Amyloidosis
|
Aminoacylase 1 Deficiency
|
Neoplasms, Glandular And Epithelial
|
Nephritis
|
Nephroblastomatosis, Fetal Ascites, Macrosomia And Wilms Tumor
|
Nephrocalcinosis
|
Nephrogenic Fibrosing Dermopathy
|
Nephrolithiasis
|
Nephronophthisis 7
|
Weill-Marchesani Syndrome
|
Neural Tube Defect, Folate-Sensitive
|
Amelogenesis Imperfecta, Hypomaturation Type, Iia2
|
Ameloblastoma
|
Neurodevelopmental Disorders
|
Neuroectodermal Tumors, Primitive, Peripheral
|
Neurofibroma
|
Werner Syndrome
|
Neutropenia
|
Neutropenia, Nonimmune Chronic Idiopathic, Adult
|
Neutropenia, Severe Congenital, Autosomal Dominant 1
|
Neutropenia, Severe Congenital, Autosomal Dominant 2
|
Nevo Syndrome
|
Nevus, Pigmented
|
Niemann-Pick Diseases
|
Niemann-Pick Disease, Type A
|
Niemann-Pick Disease, Type B
|
Night Blindness, Congenital Stationary, Autosomal Dominant 1
|
Night Blindness, Congenital Stationary, Autosomal Dominant 2
|
Night Blindness, Congenital Stationary, Autosomal Dominant 3
|
Nijmegen Breakage Syndrome-Like Disorder
|
Amaurosis Congenita Of Leber, Type 2
|
Noonan Syndrome 5
|
No-Reflow Phenomenon
|
Norman Roberts Lissencephaly Syndrome
|
Nose Neoplasms
|
Alveolitis, Extrinsic Allergic
|
Obesity, Morbid
|
Obsessive-Compulsive Disorder
|
Occipital Horn Syndrome
|
Alveolar Capillary Dysplasia
|
Ocular Hypertension
|
Oculocutaneous Albinism Type 1
|
Oculocutaneous Albinism Type 1b
|
Oculocutaneous Albinism Type 3
|
Oculootoradial Syndrome
|
Oculopalatoskeletal Syndrome
|
Oligomenorrhea
|
Opioid-Related Disorders
|
Hypertelorism With Esophageal Abnormality And Hypospadias
|
Optic Atrophy, Hereditary, Leber
|
Optic Atrophy Polyneuropathy Deafness
|
Optic Neuritis
|
Alveolar Bone Loss
|
Orofacial Cleft 1
|
Neurocirculatory Asthenia
|
Osler-Rendu-Weber Syndrome 2
|
Osseous Heteroplasia, Progressive
|
Ossification, Heterotopic
|
Ossification Of The Posterior Longitudinal Ligament Of The Spine
|
Wernicke Encephalopathy
|
Osteoarthritis With Mild Chondrodysplasia
|
Wet Macular Degeneration
|
Osteogenesis Imperfecta, Type Viii
|
Osteolysis
|
Osteolysis Hereditary Multicentric
|
Osteonecrosis
|
Osteopetrosis, Autosomal Recessive 6
|
Osteopetrosis, Autosomal Recessive 7
|
Osteopetrosis With Renal Tubular Acidosis
|
Sleep Deprivation
|
Alpha-Thalassemia Myelodysplasia Syndrome
|
Osteoporosis, Postmenopausal
|
Alpha-Mannosidosis
|
Otofaciocervical Syndrome
|
Alpha-Ketoglutarate Dehydrogenase Deficiency
|
Ovarian Diseases
|
Alpha-Beta T-Cell Lymphopenia With Gamma-Delta T-Cell Expansion, Severe Cytomegalovirus Infection, And Autoimmunity
|
Alpha-B Crystallinopathy
|
Pain Insensitivity, Congenital
|
Pallister-Hall Syndrome
|
Alopecia Universalis
|
Alopecia Areata
|
Panic Disorder
|
Papilloma, Choroid Plexus
|
Paragangliomas 3
|
18-Hydroxylase Deficiency
|
Paraplegia
|
Paraquat Lung
|
Allanson Pantzar Mcleod Syndrome
|
Parkinson Disease 4, Autosomal Dominant Lewy Body
|
Parkinson Disease 6, Autosomal Recessive Early-Onset
|
Williams Syndrome
|
Alkaptonuria
|
Parkinsonism-Dystonia, Infantile
|
Paroxysmal Nonkinesigenic Dyskinesia
|
Pediatric Obesity
|
Peeling Skin Syndrome
|
Peeling Skin Syndrome, Acral Type
|
Pemphigus, Benign Familial
|
Pena Shokeir Syndrome, Type 1
|
Penile Diseases
|
Penile Neoplasms
|
Pericardial Effusion
|
Alexander Disease
|
Peripheral Vascular Diseases
|
Persian Gulf Syndrome
|
Persistent Fetal Circulation Syndrome
|
Persistent Müllerian Duct Syndrome
|
Personality Disorders
|
Peters Anomaly
|
Peutz-Jeghers Syndrome
|
Pharyngeal Neoplasms
|
Hyperphenylalaninemia, Bh4-Deficient, C
|
Albright's Hereditary Osteodystrophy
|
Phobic Disorders
|
Phosphoenolpyruvate Carboxykinase 2 Deficiency
|
Phosphoenolpyruvate Carboxykinase Deficiency
|
Phosphoribosylpyrophosphate Synthetase Superactivity
|
Pierre Robin Syndrome With Fetal Chondrodysplasia
|
Pigmentation Disorders
|
Pigmented Nodular Adrenocortical Disease, Primary, 2
|
Pitt-Hopkins Syndrome
|
Pituitary Acth Hypersecretion
|
Pituitary Dwarfism 1
|
Pituitary Hormone Deficiency, Combined, 2
|
Pituitary Hormone Deficiency, Combined, 4
|
Pituitary Neoplasms
|
Plaque, Amyloid
|
Plaque, Atherosclerotic
|
Platyspondylic Lethal Skeletal Dysplasia, Torrance Type
|
Pleural Diseases
|
Pleuropulmonary Blastoma
|
Albinism, Oculocutaneous
|
Pneumonia, Aspiration
|
Pneumonia, Viral
|
Polycystic Kidney Diseases
|
Polycystic Liver Disease
|
Albinism Ocular Late Onset Sensorineural Deafness
|
Polycythemia Vera
|
Polydactyly
|
Polydactyly, Postaxial
|
Polydactyly, Preaxial 4
|
Polyendocrinopathies, Autoimmune
|
Polymorphic Catecholergic Ventricular Tachycardia
|
Polymyositis
|
Polyostotic Osteolytic Dysplasia, Hereditary Expansile
|
Polyploidy
|
Polyposis Syndrome, Hereditary Mixed, 2
|
Polyps
|
Polyuria
|
Porphyria, Acute Hepatic
|
Porphyria Cutanea Tarda
|
Porphyrias, Hepatic
|
Port-Wine Stain
|
Potocki-Lupski Syndrome
|
Aland Island Eye Disease
|
Precocious Puberty, Central
|
Aicardi-Goutieres Syndrome 5
|
Aicardi-Goutieres Syndrome 4
|
Agricultural Workers' Diseases
|
Pregnancy Complications
|
Agranulocytosis
|
Premature Ovarian Failure 7
|
Prickle1-Related Progressive Myoclonic Epilepsy With Ataxia
|
Primary Myelofibrosis
|
Primrose Syndrome
|
Prion Disease
|
Progressive External Ophthalmoplegia With Mitochondrial Dna Deletions, Autosomal Dominant, 5
|
Prolidase Deficiency
|
Propionic Acidemia
|
Propping Zerres Syndrome
|
Agammaglobulinemia
|
Sleep Disorders, Circadian Rhythm
|
Insomnia
|
Sleep Wake Disorders
|
Prostatic Neoplasms, Castration-Resistant
|
Adult-Onset Citrullinemia Type 2
|
Protoporphyria, Erythropoietic
|
Pseudohypoparathyroidism
|
Pseudohypoparathyroidism Type 1b
|
Pseudopseudohypoparathyroidism
|
Psychomotor Agitation
|
Psychomotor Disorders
|
Adrenocortical Carcinoma, Hereditary
|
Adrenal Hyperplasia, Congenital, Type 5
|
Pulmonary Veno-Occlusive Disease
|
Purine-Pyrimidine Metabolism, Inborn Errors
|
Purpura, Thrombocytopenic, Idiopathic
|
Purpura, Thrombotic Thrombocytopenic
|
Pyloric Stenosis, Infantile Hypertrophic 1
|
Pyropoikilocytosis, Hereditary
|
Leigh Necrotizing Encephalopathy Due To Pyruvate Carboxylase Deficiency
|
Pyruvate Dehydrogenase Phosphatase Deficiency
|
Pyruvate Kinase Deficiency Of Red Cells
|
Radiation Injuries
|
Raine Syndrome
|
Rapadilino Syndrome
|
Rapp-Hodgkin Syndrome
|
Reflex, Abnormal
|
Refsum Disease
|
Refsum Disease, Infantile
|
Winkelman Bethge Pfeiffer Syndrome
|
Chronic Kidney Disease
|
Respiration Disorders
|
Adjustment Disorders
|
Respiratory Insufficiency
|
Respiratory Syncytial Virus Infections
|
Reticulocytosis
|
Retinal Cone Dystrophy 4
|
Adenosine Triphosphate, Elevated, Of Erythrocytes
|
Retinal Detachment
|
Adenosine Monophosphate Deaminase Deficiency
|
Retinal Dystrophies
|
Adenoma, Oxyphilic
|
Retinitis Pigmentosa 10
|
Retinitis Pigmentosa 31
|
Retinitis Pigmentosa 37
|
Retinitis Pigmentosa 4
|
Retinitis Pigmentosa 9
|
Rett Syndrome
|
Rhabdomyosarcoma
|
Rhabdomyosarcoma, Alveolar
|
Rhabdomyosarcoma, Embryonal
|
Rhinitis, Allergic, Perennial
|
Riddle Syndrome
|
Roberts Syndrome
|
Robinow Syndrome, Autosomal Recessive
|
Rothmund-Thomson Syndrome
|
Rupture, Spontaneous
|
Sagittal Sinus Thrombosis
|
Salivary Gland Adenoma, Pleomorphic
|
Adenoma, Liver Cell
|
Sarcoidosis
|
Sarcoma Family Syndrome Of Li And Fraumeni
|
Scapuloperoneal Myopathy, X-Linked Dominant
|
Adenocarcinoma, Follicular
|
Scoliosis
|
Seborrhea-Like Dermatitis With Psoriasiform Elements
|
Segawa Syndrome, Autosomal Recessive
|
Adenocarcinoma, Clear Cell
|
Febrile Seizures
|
Acth-Secreting Pituitary Adenoma
|
Serum Sickness
|
Severe Acute Respiratory Syndrome
|
Severe Combined Immunodeficiency Due To Adenosine Deaminase Deficiency
|
Dengue Hemorrhagic Fever
|
Sexual Dysfunctions, Psychological
|
Sexual Infantilism
|
Acro-Osteolysis
|
Shock, Cardiogenic
|
Shock, Hemorrhagic
|
Septic Shock
|
Short Rib-Polydactyly Syndrome
|
Short Stature, Idiopathic, Autosomal
|
N-Acetylneuraminic Acid Storage Disease
|
Single Upper Central Incisor
|
Situs Inversus
|
Wittwer Syndrome
|
Skeletal Defects, Genital Hypoplasia, And Mental Retardation
|
Wolfram Syndrome 2
|
Acromicric Dysplasia
|
Acrocapitofemoral Dysplasia
|
Smith-Magenis Syndrome
|
Solitary Fibrous Tumors
|
Sotos Syndrome
|
Spasms, Infantile
|
Spastic Paraplegia 15, Autosomal Recessive
|
Spastic Paraplegia 33, Autosomal Dominant
|
Spastic Paraplegia 7, Autosomal Recessive
|
Spastic Paraplegia, Hereditary
|
Spastic Paraplegia 5a, Autosomal Recessive
|
Speech Disorders
|
Spherocytosis, Hereditary
|
Spherocytosis, Type 3
|
Spinal Cord Injuries
|
Spinal Dysraphism
|
Spinal Muscular Atrophy, Distal, X-Linked 3
|
Spinal Muscular Atrophy With Respiratory Distress 1
|
Spinocerebellar Ataxia 14
|
Spinocerebellar Ataxia 17
|
Spinocerebellar Ataxia 28
|
Spinocerebellar Ataxia, Autosomal Recessive 5
|
Splenic Diseases
|
Xanthinuria, Type I
|
Split-Hand-Foot Malformation 4
|
Spondyloenchondrodysplasia
|
Spondyloepimetaphyseal Dysplasia, Aggrecan Type
|
Spondyloepimetaphyseal Dysplasia, Missouri Type
|
Spondyloepiphyseal Dysplasia, Congenita
|
Spondyloepiphyseal Dysplasia, Kimberley Type
|
Spondylometaphyseal Dysplasia, Kozlowski Type
|
Spongiform Encephalopathy With Neuropsychiatric Features
|
Staphylococcal Infections
|
Starvation
|
Acrocallosal Syndrome
|
Acidosis, Lactic
|
Stickler Syndrome, Type 1
|
Stickler Syndrome, Type 2
|
Stickler Syndrome, Type 3
|
Stickler Syndrome, Type I, Nonsyndromic Ocular
|
Stomach Diseases
|
Achondrogenesis Type 2
|
Acatalasia
|
Striatal Degeneration, Autosomal Dominant
|
Strudwick Syndrome
|
Sturge-Weber Syndrome
|
Subarachnoid Hemorrhage
|
Carcinoid Tumors, Intestinal
|
Sudden Infant Death
|
Sulfite Oxidase Deficiency
|
Sunburn
|
Sweat Gland Neoplasms
|
Synovitis
|
Tachycardia, Sinus
|
Takayasu Arteritis
|
Tarp Syndrome
|
Telangiectasia, Hereditary Hemorrhagic
|
Temporomandibular Joint Disorder
|
Testicular Diseases
|
Abnormalities, Drug-Induced
|
Testicular Neoplasms
|
Tetralogy Of Fallot
|
Thoracic Diseases
|
Thrombasthenia
|
Abdominal Obesity Metabolic Syndrome
|
Thrombocytopenia 4
|
Thrombocytopenia, Platelet Dysfunction, Hemolysis, And Imbalanced Globin Synthesis
|
Activated Protein C Resistance
|
Thrombophilia Due To Elevated Histidine-Rich Glycoprotein
|
Thrombophilia, Hereditary
|
Thrombophilia, X-Linked, Due To Factor Ix Defect
|
Aarskog Syndrome
|
Thrombotic Microangiopathies
|
Thymus Neoplasms
|
Thyroid Cancer, Follicular
|
Thyroid Carcinoma, Anaplastic
|
Thyroid Dyshormonogenesis 2a
|
Thyroid Hormone Resistance, Generalized, Autosomal Dominant
|
Thyroid Hormone Resistance, Generalized, Autosomal Recessive
|
Thyroid Hormone Resistance, Selective Pituitary
|
Thyroid Hormone Resistance Syndrome
|
Thyroiditis, Autoimmune
|
6-Pyruvoyl-Tetrahydropterin Synthase Deficiency
|
Tic Disorders
|
Tight Skin Contracture Syndrome, Lethal
|
Timothy Syndrome
|
Nicotine Dependence
|
46,Xy Gonadal Dysgenesis, Partial, With Minifascicular Neuropathy
|
Townes-Brocks Syndrome
|
Transient Myeloproliferative Disorder Of Down Syndrome
|
Trauma, Nervous System
|
Tremor
|
Trichorhinophalangeal Syndrome, Type I
|
Trichorhinophalangeal Syndrome, Type Iii
|
Trichuriasis
|
Hyperostosis-Hyperphosphatemia Syndrome
|
46,Xy Gonadal Dysgenesis, Complete Or Partial, Dhh-Related
|
Xanthomatosis, Cerebrotendinous
|
Ureteral Obstruction
|
Uridine 5-Prime Monophosphate Hydrolase Deficiency, Hemolytic Anemia Due To
|
Urinary Bladder Neck Obstruction
|
Urinary Tract Infections
|
Urination Disorders
|
Urogenital Abnormalities
|
Urogenital Neoplasms
|
Urologic Neoplasms
|
Usher Syndrome, Type 1d
|
46, Xx Disorders Of Sex Development
|
Uterine Neoplasms
|
Cardiomyopathy, Familial Hypertrophic, 10
|
Cardiomyopathy, Familial Hypertrophic, 13
|
Cardiomyopathy, Familial Hypertrophic, 4
|
Cardiomyopathy, Familial Restrictive, 1
|
Cardiomyopathy, Familial Hypertrophic, 1
|
Cardiomyopathy, Restrictive
|
Cardiotoxicity
|
Cardiomyopathy, Dilated, 2a
|
Cardiovirus Infections
|
Carnevale Syndrome
|
Carotid Artery Thrombosis
|
Carotid Intimal Medial Thickness 1
|
Cataract And Cardiomyopathy
|
Cayler Cardiofacial Syndrome
|
Cecal Neoplasms
|
Cardiomyopathy, Dilated, 1z
|
Central Nervous System Diseases
|
Central Nervous System Neoplasms
|
Cerebellar Ataxia, Mental Retardation, And Dysequilibrium Syndrome 3
|
Cerebellar Diseases
|
Cerebral Amyloid Angiopathy
|
Cerebral Amyloid Angiopathy, App-Related
|
Cardiomyopathy, Dilated, 1m
|
Cerebral Hemorrhage With Amyloidosis, Hereditary, Dutch Type
|
Cerebrooculofacioskeletal Syndrome 1
|
Cerebrooculofacioskeletal Syndrome 2
|
Ceroid Lipofuscinosis, Neuronal, 2
|
Charcot-Marie-Tooth Disease
|
Charcot-Marie-Tooth Disease, Axonal, Type 2n
|
Charcot-Marie-Tooth Disease, Type 1d
|
Charcot-Marie-Tooth Disease, Axonal, With Vocal Cord Paresis, Autosomal Recessive
|
Charcot-Marie-Tooth Disease, Type 4e
|
Charcot-Marie-Tooth Disease, Type 4h
|
Cardiomyopathy, Dilated, 1j
|
Cardiomyopathy, Dilated, 1ff
|
Cardiomyopathy, Dilated, 1c
|
Sclerosing Cholangitis
|
Cholestasis, Progressive Familial Intrahepatic 1
|
Chondrodysplasia, Acromesomelic, With Genital Anomalies
|
Chondrodysplasia Punctata, Brachytelephalangic
|
Chorea
|
Chromosome 17 Deletion
|
Chromosome 2q37 Deletion Syndrome
|
Chromosome Aberrations
|
Chronobiology Disorders
|
Chylomicron Retention Disease
|
Cardiomyopathy, Dilated, 1bb
|
Clubfoot
|
Cardiomyopathy, Dilated, 1aa
|
Cardioencephalomyopathy, Fatal Infantile, Due To Cytochrome C Oxidase Deficiency
|
Coloboma
|
Carcinoma, Lobular
|
Colorectal Adenomatous Polyposis, Autosomal Recessive
|
Dyskinesias
|
Carcinoma, Intraductal, Noninfiltrating
|
Colorectal Neoplasms, Hereditary Nonpolyposis
|
Color Vision Defects
|
Coma
|
Compartment Syndromes
|
Complement Factor I Deficiency
|
Cone Dystrophy 3
|
Cone Dystrophy 4
|
Cone-Rod Dystrophy 5
|
Cone-Rod Dystrophy 7
|
Cone-Rod Dystrophy, X-Linked, 3
|
Varicose Veins
|
Congenital Adrenal Hyperplasia Due To 21 Hydroxylase Deficiency
|
Congenital Amegakaryocytic Thrombocytopenia
|
Congenital Disorder Of Glycosylation Type 1b
|
Congenital Disorder Of Glycosylation Type 2d
|
Congenital Hypothyroidism
|
Constipation
|
Contracture
|
Corneal Diseases
|
Corneal Dystrophy, Fleck
|
Corneal Dystrophy, Fuchs Endothelial, 6
|
Corneal Dystrophy, Posterior Polymorphous, 1
|
Corneal Dystrophy, Posterior Polymorphous, 3
|
Carcinoma In Situ
|
Coronary Stenosis
|
Cough
|
Coumarin Resistance
|
Coxsackievirus Infections
|
Carcinoma, Ductal
|
Craniopharyngioma
|
Craniosynostosis Radial Aplasia Syndrome
|
Creutzfeldt Jacob Disease
|
Cri-Du-Chat Syndrome
|
Critical Illness
|
Cryopyrin-Associated Periodic Syndromes
|
Cytochrome-C Oxidase Deficiency
|
Darier Disease
|
Deafness, Autosomal Dominant 10
|
Deafness, Autosomal Dominant 13
|
Deafness, Autosomal Recessive 35
|
Deafness, Autosomal Recessive 53
|
Deafness, X-Linked 1
|
Death, Sudden
|
Sudden Cardiac Arrest
|
Delayed Emergence From Anesthesia
|
3-Methylcrotonyl Coa Carboxylase 1 Deficiency
|
Dengue
|
Denys-Drash Syndrome
|
Deoxyguanosine Kinase Deficiency
|
Carboxypeptidase N Deficiency
|
Carbon Tetrachloride Poisoning
|
Carbamoyl-Phosphate Synthase I Deficiency Disease
|
Capillary Malformation-Arteriovenous Malformation
|
Candidiasis, Vulvovaginal
|
Dermatomyositis
|
Desbuquois Syndrome
|
Dextrocardia
|
Vasculitis
|
Diabetes Insipidus, Nephrogenic
|
Candidiasis, Oral
|
Candidiasis, Familial, 2
|
Diabetes Mellitus, Insulin-Dependent, 19
|
Diabetes Mellitus, Neonatal, With Congenital Hypothyroidism
|
Candidiasis
|
Canavan Disease
|
Calcification Of Joints And Arteries
|
Diabetic Cardiomyopathies
|
Cafe-Au-Lait Spots
|
Vasculopathy, Retinal, With Cerebral Leukodystrophy
|
Xeroderma Pigmentosum, Complementation Group D
|
Diaphragmatic Hernia 3
|
Diarrhea
|
Digeorge Syndrome
|
Dihydropyrimidinase Deficiency
|
Dihydropyrimidine Dehydrogenase Deficiency
|
Burns, Chemical
|
Distal Arthrogryposis Type 2b
|
Distal Myopathies
|
Distal Myopathy, Nonaka Type
|
Dog Diseases
|
Donnai-Barrow Syndrome
|
Dopamine Beta Hydroxylase Deficiency
|
Xeroderma Pigmentosum, Complementation Group G
|
Ventricular Dysfunction
|
Dry Eye Syndromes
|
3-Hydroxy-3-Methylglutaryl-Coa Lyase Deficiency
|
Dwarfism
|
Dysarthria
|
Dyssegmental Dysplasia
|
Dyssomnias
|
Bulbospinal Neuronopathy, X-Linked Recessive
|
Dystonia 12
|
Dystonia 6, Torsion
|
Dystonia, Dopa-Responsive
|
Early-Onset Ataxia With Oculomotor Apraxia And Hypoalbuminemia
|
Echinococcosis
|
Ectodermal Dysplasia, Anhidrotic, With Immunodeficiency, Osteopetrosis, And Lymphedema
|
Ectodermal Dysplasia, Ectrodactyly, And Macular Dystrophy
|
Ectodermal Dysplasia, Hypohidrotic, With Immune Deficiency
|
Ectrodactyly-Cleft Lip-Palate Syndrome
|
Ectrodactyly, Ectodermal Dysplasia, And Cleft Lip-Palate Syndrome 3
|
Ventricular Premature Complexes
|
Ehlers-Danlos Syndrome
|
Ehlers-Danlos Syndrome, Cardiac Valvular Form
|
Ehlers-Danlos Syndrome, Progeroid Form
|
Ehlers-Danlos Syndrome Type 2
|
Ehlers-Danlos Syndrome Type 3
|
Ehlers-Danlos Syndrome Type 6
|
Ehlers-Danlos Syndrome, Type Vii, Autosomal Recessive
|
Elliptocytosis 2
|
Embryo Loss
|
Encephalitis
|
Endocrine-Cerebroosteodysplasia
|
Endometrial Hyperplasia
|
Bruton Type Agammaglobulinemia
|
End Stage Liver Disease
|
Enhanced S-Cone Syndrome
|
Brugada Syndrome 3
|
Eosinophilia
|
Ependymoma
|
Epidermolysis Bullosa With Pyloric Atresia
|
Bruck Syndrome 2
|
Epilepsy, Idiopathic Generalized
|
Epilepsy, Rolandic
|
Epiphyseal Dysplasia, Multiple, With Myopia And Conductive Deafness
|
Episodic Ataxia, Type 2
|
Erectile Dysfunction
|
Erythema
|
Erythema Multiforme
|
Erythrocytosis, Familial, 3
|
Esophageal Diseases
|
Bronchopulmonary Dysplasia
|
Esophageal Stenosis
|
Ethylmalonic Encephalopathy
|
Extravasation Of Diagnostic And Therapeutic Materials
|
Bronchial Diseases
|
Eye Diseases
|
Facial Asymmetry
|
Facies
|
Factor 8 Deficiency, Acquired
|
Factor V Deficiency
|
Factor Xiii, A Subunit, Deficiency Of
|
Factor Xiii Deficiency
|
Familial Apoceruloplasmin Deficiency
|
Familial Cylindromatosis
|
Familial Hypophosphatemic Rickets
|
Familial Mediterranean Fever
|
Familial Mediterranean Fever, Autosomal Dominant
|
Fanconi Anemia, Complementation Group J
|
Farber Lipogranulomatosis
|
Fatigue
|
Brody Myopathy
|
Brittle Cornea Syndrome 1
|
Feminization
|
Femur Head Necrosis
|
Vesicular Stomatitis
|
Fibroadenoma
|
Fibroma
|
Fibrous Dysplasia Of Bone
|
Fibrous Dysplasia, Polyostotic
|
Flushing
|
Fractures, Closed
|
Fragile X Syndrome
|
Frasier Syndrome
|
Friedreich Ataxia
|
Friedreich Ataxia 1
|
Fructose-1,6-Diphosphatase Deficiency
|
Fundus Albipunctatus
|
Fundus Dystrophy, Pseudoinflammatory, Of Sorsby
|
Gait Disorders, Neurologic
|
Galactosemias
|
Gallbladder Neoplasm
|
Gallstones
|
Gamma Aminobutyric Acid Transaminase Deficiency
|
Gastrointestinal Hemorrhage
|
Gastrointestinal Neoplasms
|
Gastroparesis
|
Generalized Epilepsy And Paroxysmal Dyskinesia
|
Genetic Diseases, Inborn
|
Genital Diseases, Male
|
Amyloidosis, Cerebral, With Spongiform Encephalopathy
|
Ghosal Hematodiaphyseal Dysplasia
|
Gingival Hypertrophy
|
Glaucoma
|
Glaucoma 3, Primary Congenital, A
|
Open-Angle Glaucoma
|
Breast Diseases
|
Branchio-Oto-Renal Syndrome
|
Brain Stem Neoplasms
|
Virus Diseases
|
Membranous Glomerulonephritis
|
Glutathione Synthetase Deficiency
|
Glutathione Synthetase Deficiency Of Erythrocytes, Hemolytic Anemia Due To
|
Glycogen Storage Disease
|
Glycogen Storage Disease Type V
|
Glycogen Storage Disease Type Vii
|
Glycogen Storage Disease Xiii
|
Goiter
|
Gonadal Dysgenesis, 46,Xx
|
Gonadal Dysgenesis, 46,Xy
|
Granuloma, Plasma Cell
|
Granuloma, Respiratory Tract
|
Granulomatous Disease, Chronic, Autosomal Recessive, Cytochrome B-Negative
|
Granulomatous Disease, Chronic, X-Linked
|
Graves Disease
|
Greig Cephalopolysyndactyly Syndrome
|
Griscelli Syndrome Type 3
|
Brain Diseases, Metabolic, Inborn
|
Growth Mental Deficiency Syndrome Of Myhre
|
Growth Retardation, Developmental Delay, Coarse Facies, And Early Death
|
Hair Diseases
|
Hamartoma
|
Hamartoma Syndrome, Multiple
|
Hand Deformities, Congenital
|
Hashimoto Disease
|
Hawkinsinuria
|
Hay-Wells Syndrome
|
Hearing Loss, Conductive
|
Rickets, Hereditary Vitamin D-Resistant
|
Heartburn
|
Brachydactyly With Hypertension
|
Brachydactyly, Type B1
|
Brachydactyly Type A2
|
Heat Stroke
|
Heavy Metal Toxicity
|
Helicobacter Infections
|
Hemangioma, Capillary Infantile
|
Brachydactyly Type A1
|
Hematologic Neoplasms
|
Hematoma
|
Hematuria
|
Hemiplegic Migraine, Familial Type 1
|
Hemiplegic Migraine, Familial Type 2
|
Hemochromatosis
|
Hemolytic-Uremic Syndrome
|
Hemophagocytic Lymphohistiocytosis, Familial, 2
|
Hemophilia B
|
Hemorrhagic Disorders
|
Hemorrhoids
|
Hepatic Encephalopathy
|
Hepatitis, Animal
|
Hepatitis, Autoimmune
|
Borjeson-Forssman-Lehmann Syndrome
|
Bone Resorption
|
Bone Marrow Diseases
|
Hepatorenal Syndrome
|
Hereditary Angioedema Types I And Ii
|
Hereditary Autoinflammatory Diseases
|
Hereditary Breast And Ovarian Cancer Syndrome
|
Hereditary Pancreatitis
|
Hereditary Renal Agenesis
|
Hereditary Sensory And Autonomic Neuropathies
|
Hereditary Sensory And Motor Neuropathy
|
Bone Fragility With Contractures, Arterial Rupture, And Deafness
|
Hernia, Inguinal
|
Heterotaxy, Visceral, 5, Autosomal
|
Hirschsprung Disease
|
Histiocytoma, Benign Fibrous
|
Hiv-Associated Lipodystrophy Syndrome
|
Hiv Seropositivity
|
Hodgkins Lymphoma
|
Cyclopia
|
Holoprosencephaly 3
|
Holoprosencephaly 5
|
Holoprosencephaly 9
|
Homocarnosinosis
|
Homocystinuria
|
Hoyeraal Hreidarsson Syndrome
|
Huntington Disease-Like 1
|
Hyalinosis, Systemic
|
Hyaloideoretinal Degeneration Of Wagner
|
Vitamin D Hydroxylation-Deficient Rickets, Type 1a
|
Bohring Syndrome
|
Hyperammonemia
|
Hyperandrogenism
|
Hyperargininemia
|
Hypercalciuria
|
Hypercalciuria, Absorptive, 2
|
Hypercarotenemia And Vitamin A Deficiency, Autosomal Dominant
|
Blood Platelet Disorders
|
Vitamin D Hydroxylation-Deficient Rickets, Type 1b
|
Hyper-Igm Immunodeficiency Syndrome
|
Hyperkalemia
|
Hyperkeratosis, Epidermolytic
|
Blister
|
Hypermethioninemia
|
Hyperostosis, Cortical, Congenital
|
Hyperoxia
|
Hyperphenylalaninemia, Bh4-Deficient, B
|
Hyperphosphatemia
|
Blindness
|
Blast Crisis
|
Hypersensitivity, Delayed
|
Hypersensitivity, Immediate
|
Biotinidase Deficiency
|
Hypertension, Early-Onset, Autosomal Dominant, With Severe Exacerbation In Pregnancy
|
Bile Duct Diseases
|
Hypertension, Malignant
|
Hypertension, Portal
|