Liver Cirrhosis, Experimental
|
Prostatic Neoplasms
|
Breast Carcinoma
|
Hypertension
|
Hepatocellular Carcinoma
|
Obesity
|
Stomach Neoplasms
|
Drug-Induced Liver Injury
|
Rheumatoid Arthritis
|
Colorectal Cancer
|
Melanoma
|
Myocardial Ischemia
|
Neoplasm Metastasis
|
Autism
|
Endometriosis
|
Lung Neoplasms
|
Inflammation
|
Alzheimer's Disease
|
Diabetes Mellitus, Type 2
|
Intellectual Disability
|
Myocardial Infarction
|
Neoplasm Invasiveness
|
Mammary Neoplasms, Experimental
|
Colonic Neoplasm
|
Disease Progression
|
Craniofacial Abnormalities
|
Drug Dependence
|
Carcinoma
|
Liver Neoplasms
|
Renal Cell Carcinoma
|
Fatty Liver
|
Diabetes Mellitus, Experimental
|
Urinary Bladder Neoplasms
|
Osteoarthritis
|
Heart Failure
|
Heart Diseases
|
Coronary Artery Disease
|
Carcinoma, Non-Small-Cell Lung
|
Mesothelioma, Malignant
|
Asthma
|
Ovarian Neoplasms
|
Myocardial Reperfusion Injury
|
Peripheral Neuropathy
|
Nerve Degeneration
|
Mammary Neoplasms, Animal
|
Reperfusion Injury
|
Intracerebral Hemorrhage
|
Dermatitis, Contact
|
Thrombosis
|
Seizures
|
Cardiac Hypertrophy
|
Osteoporosis
|
Skin Diseases
|
Abortion, Spontaneous
|
Hiv Infections
|
Adenocarcinoma
|
Psoriasis
|
Liver Cirrhosis
|
Recurrence
|
Drug-Related Side Effects And Adverse Reactions
|
Disease Models, Animal
|
Anoxia
|
Polycystic Ovary Syndrome
|
Insulin Resistance
|
Amphetamine-Related Disorders
|
Kidney Disease
|
Cocaine Dependence
|
Brain Ischemia
|
Stroke
|
Squamous Cell Carcinoma
|
Systemic Lupus Erythematosus
|
Liver Diseases
|
Schizophrenia
|
Genetic Predisposition To Disease
|
Calcinosis
|
Non-Alcoholic Fatty Liver Disease
|
Glioblastoma Multiforme
|
Neuroblastoma
|
Status Epilepticus
|
Venous Thrombosis
|
Arthritis, Juvenile
|
Left Ventricular Hypertrophy
|
Thromboembolism
|
Cell Transformation, Neoplastic
|
Proteinuria
|
Idiopathic Pulmonary Fibrosis
|
Brain Injuries
|
Diabetic Nephropathy
|
Hemorrhage
|
Learning Disorders
|
Hypotension
|
Arsenic Poisoning
|
Albuminuria
|
Respiratory Distress Syndrome, Adult
|
Weight Gain
|
Carcinoma, Transitional Cell
|
Acute Kidney Injury
|
Neurotoxicity Syndromes
|
Pancreatic Carcinoma
|
Atherosclerosis
|
Acute Coronary Syndrome
|
Pancreatitis, Chronic
|
Male Infertility
|
Parkinson's Disease
|
Leukemia, Myeloid, Acute
|
Iga Glomerulonephritis
|
Ulcerative Colitis
|
Nervous System Diseases
|
Aicardi-Goutieres Syndrome
|
Mouth Neoplasms
|
Hepatitis
|
Hepatolenticular Degeneration
|
Lung Adenocarcinoma
|
Muscular Diseases
|
Nasopharyngeal Carcinoma
|
Necrosis
|
Neoplasms
|
Diabetic Neuropathies
|
Neurodegenerative Diseases
|
Hyperlipidemias
|
Hypercholesterolemia, Familial
|
Dyslipidemias
|
Pulmonary Hypertension
|
Organophosphate Poisoning
|
Bone Neoplasms
|
Parkinsonian Disorders
|
Brain Diseases
|
Infarction, Middle Cerebral Artery
|
Influenza, Human
|
Precancerous Conditions
|
Amyotrophic Lateral Sclerosis 1
|
Prenatal Injuries
|
Chronic Obstructive Pulmonary Disease
|
Pulmonary Emphysema
|
Pulmonary Fibrosis
|
Leukemia
|
Coronary Heart Disease
|
Glioma
|
Liver Neoplasms, Experimental
|
Skin Neoplasms
|
Carcinoma, Adenoid Cystic
|
Lung Diseases
|
Lymphoma
|
Carcinoma, Squamous Cell Of Head And Neck
|
Autoimmune Disease
|
Memory Disorders
|
Metabolic Syndrome X
|
Ventricular Dysfunction, Left
|
Cardiovascular Disease
|
Dermatitis, Allergic Contact
|
Retinal Detachment
|
Retinal Diseases
|
Neointima
|
Substance Withdrawal Syndrome
|
Hepatitis C
|
Jaw Abnormalities
|
Cone-Rod Dystrophy 2
|
Primary Biliary Cirrhosis
|
Sezary Syndrome
|
Developmental Disabilities
|
Intracranial Hemorrhages
|
Testicular Neoplasms
|
Acute Lymphoblastic Leukemia
|
Fibrosis
|
Unipolar Depression
|
Ovarian Cysts
|
Pulmonary Embolism
|
Myoclonic Epilepsies, Progressive
|
Diabetes Mellitus, Type 1
|
Myelodysplastic Syndromes
|
Skin Abnormalities
|
Aortic Rupture
|
Hypertrophy
|
Microcephaly
|
Micronuclei, Chromosome-Defective
|
Meningioma
|
Esophageal Neoplasms
|
Astrocytoma
|
Basal Cell Carcinoma
|
Dilated Cardiomyopathy
|
Hematuria
|
Ceroid Lipofuscinosis, Neuronal 1, Infantile
|
Metabolism, Inborn Errors
|
Hypercholesterolemia
|
Anemia
|
Multiple Sclerosis
|
Preeclampsia
|
Disseminated Intravascular Coagulation
|
Kidney Neoplasms
|
Gaucher Disease
|
Endometrial Neoplasm
|
Limb Dystonia
|
Venous Thromboembolism
|
Edema
|
Neural Tube Defects
|
Pancreatitis
|
Amino Acid Metabolism, Inborn Errors
|
Nephrosis
|
Splenomegaly
|
Age-Related Macular Degeneration
|
Epilepsy
|
Arterial Occlusive Diseases
|
Lipidoses
|
Sepsis
|
Pneumonia
|
Cerebral Infarction
|
Familial Primary Pulmonary Hypertension
|
Toxic Epidermal Necrolysis
|
Diabetic Retinopathy
|
Graves Disease
|
Paralysis
|
Growth Disorders
|
Coronary Restenosis
|
Neurologic Manifestations
|
Neuroendocrine Tumors
|
Mucopolysaccharidosis Iv
|
Neuroectodermal Tumors, Primitive
|
Small Cell Lung Carcinoma
|
Lung Injury
|
Adenoma
|
Lupus Nephritis
|
Angina, Unstable
|
Lymphoma, Follicular
|
Attention Deficit Hyperactivity Disorder
|
Lymphoma, Non-Hodgkin
|
Glucose Intolerance
|
Lymphoma, T-Cell, Cutaneous
|
Atypical Hemolytic Uremic Syndrome
|
Macular Degeneration, Age-Related, 1
|
Autism Spectrum Disorder
|
Hyperalgesia
|
Neoplasms, Germ Cell And Embryonal
|
Huntington Disease
|
Hodgkins Lymphoma
|
Mandibular Diseases
|
Cryptorchidism
|
Wounds And Injuries
|
Diabetic Cardiomyopathies
|
Marfan Syndrome
|
Amenorrhea
|
Angioedema
|
Heart Defects, Congenital
|
Thrombocytopenia
|
Myopathies, Structural, Congenital
|
Thrombophilia
|
Thymoma
|
Thyroid Cancer, Follicular
|
Hernia, Diaphragmatic
|
Muscular Dystrophies
|
Motor Skills Disorders
|
Tremor
|
Alternating Hemiplegia Of Childhood
|
Meningococcal Infection
|
Heart Valve Diseases
|
Hereditary Pancreatitis
|
Muscle Rigidity
|
Urologic Neoplasms
|
Uterine Cervical Neoplasms
|
Aging, Premature
|
Hemangiosarcoma
|
Vascular System Injuries
|
Penile Diseases
|
Endometrial Hyperplasia
|
Periodontitis
|
Parkinson Disease, Secondary
|
Endomyocardial Fibrosis
|
Brain Edema
|
Brain Infarction
|
Mesothelioma
|
Enterocolitis, Necrotizing
|
Cholestasis, Progressive Familial Intrahepatic 1
|
Paresis
|
Pneumoconiosis
|
Pneumonia, Pneumococcal
|
Inflammatory Bowel Disease
|
Diabetes Mellitus
|
Poisoning
|
Amyotrophic Lateral Sclerosis
|
Ichthyosis
|
Embolism, Cholesterol
|
Intracranial Embolism And Thrombosis
|
Postoperative Complications
|
Cardiomyopathy, Hypertrophic
|
Brain Neoplasms
|
Chromosome Aberrations
|
Premature Birth
|
Arteritis
|
Amelogenesis Imperfecta, Hypomaturation Type, Iia1
|
Ischemia
|
Ischemic Attack, Transient
|
Eye Abnormalities
|
Eye Diseases, Hereditary
|
Pain
|
Cholangiocarcinoma
|
Coffin-Siris Syndrome
|
Hypotonia-Cystinuria Syndrome
|
Arthritis, Experimental
|
Colitis
|
Amyloidosis
|
Chilblain Lupus 1
|
Atopic Eczema
|
Hepatitis, Chronic
|
Kidney Failure, Chronic
|
Bone Diseases, Developmental
|
Lactose Intolerance, Adult Type
|
Fanconi Anemia
|
Oral Submucous Fibrosis
|
Renal Insufficiency
|
Body Weight
|
Bloom Syndrome
|
Respiratory Insufficiency
|
Hypertriglyceridemia
|
Respiratory Tract Diseases
|
Blood Coagulation Disorders
|
Reticuloendotheliosis, Familial, With Eosinophilia
|
Occupational Diseases
|
Adenomatous Polyposis Coli
|
Retinal Degeneration
|
Leopard Syndrome
|
Allanson Pantzar Mcleod Syndrome
|
Asphyxia Neonatorum
|
Acidosis, Lactic
|
Leukemia, Myeloid
|
Aortic Diseases
|
Hyperplasia
|
Thoracic Aortic Aneurysm
|
Adrenal Hyperplasia, Congenital
|
Hyperparathyroidism, Secondary
|
Systemic Scleroderma
|
Hyperlipoproteinemias
|
Drug Hypersensitivity
|
Birth Weight
|
Lipodystrophy
|
Bipolar Disorder
|
Abnormalities, Multiple
|
Hyper-Igm Immunodeficiency Syndrome
|
Alcoholic Liver Cirrhosis
|
Hyperhomocysteinemia
|
Hyperemia
|
Neuronal Ceroid-Lipofuscinoses
|
Silicosis
|
Intervertebral Disc Disease
|
Intracranial Hemorrhage, Traumatic
|
Intracranial Thrombosis
|
Intrahepatic Cholestasis Of Pregnancy
|
Iron-Refractory Iron Deficiency Anemia
|
Irritable Bowel Syndrome
|
Jaundice, Obstructive
|
Joint Diseases
|
Joubert Syndrome 1
|
Juvenile Polyposis Syndrome
|
Kallmann Syndrome
|
Keloid
|
Keratosis Palmoplantaris With Periodontopathia And Onychogryposis
|
Kufor-Rakeb Syndrome
|
Lactase Deficiency, Congenital
|
Lafora Disease
|
Language Development Disorders
|
Lead Poisoning
|
Leber Congenital Amaurosis
|
Leiomyosarcoma
|
Leishmaniasis
|
Leishmaniasis, Cutaneous
|
Leukemia, Erythroblastic, Acute
|
Leukemia, Lymphoid
|
Leukemia-Lymphoma, Adult T-Cell
|
Chronic Myelogenous Leukemia
|
Leukemia, Myelomonocytic, Juvenile
|
Leukemia, T-Cell
|
Leukodystrophy, Globoid Cell
|
Leukodystrophy, Metachromatic
|
Leukoencephalopathy, Cystic, Without Megalencephaly
|
Leukopenia
|
Lewy Body Dementia
|
Liddle Syndrome
|
Limb-Girdle Muscular Dystrophy Type 2a
|
Lipid Metabolism, Inborn Errors
|
Lipomatosis
|
Liposarcoma
|
Listeriosis
|
Liver Diseases, Alcoholic
|
Liver Failure
|
Liver Failure, Acute
|
Long Qt Syndrome
|
Low Back Pain
|
Lower Extremity Deformities, Congenital
|
Lymphoma, B-Cell
|
Lymphoma, Large B-Cell, Diffuse
|
Lymphoma, T-Cell
|
Lysosomal Acid Lipase Deficiency
|
Beta-Mannosidosis
|
Machado-Joseph Disease
|
Macrocephaly Autism Syndrome
|
Macular Degeneration, Age-Related, 7
|
Majeed Syndrome
|
Malformations Of Cortical Development
|
Malpuech Facial Clefting Syndrome
|
Mandibuloacral Dysplasia With Type A Lipodystrophy
|
Mandibuloacral Dysplasia With Type B Lipodystrophy
|
Manganese Poisoning
|
Masp2 Deficiency
|
Maturity-Onset Diabetes Of The Young, Type 8, With Exocrine Dysfunction
|
Maxillary Diseases
|
Mediastinal Neoplasms
|
Megalencephaly
|
Megalocytic Interstitial Nephritis
|
Meningioma, Familial
|
Meningoencephalitis
|
Menkes Kinky Hair Syndrome
|
Mental Retardation, Autosomal Recessive 1
|
Mental Retardation-Hypotonic Facies Syndrome, X-Linked, 1
|
Mental Retardation, X-Linked
|
Mesenteric Ischemia
|
Metabolic Diseases
|
Metachondromatosis
|
Metaphyseal Anadysplasia 2
|
Methylmalonic Aciduria Cbla Type
|
Microphthalmos
|
Microsatellite Instability
|
Mitochondrial Diseases
|
Mitochondrial Encephalomyopathies
|
Morm Syndrome
|
Morphine Dependence
|
Motor Neuron Disease
|
Mouth Abnormalities
|
Movement Disorder
|
Mucopolysaccharidosis I
|
Mucopolysaccharidosis Ii
|
Mucopolysaccharidosis Iii
|
Mucopolysaccharidosis Vi
|
Mucopolysaccharidosis Vii
|
Multiple Myeloma
|
Multiple Organ Failure
|
Muscle Weakness
|
Muscular Atrophy
|
Musculoskeletal Pain
|
Myasthenia Gravis
|
Mycoplasma Infections
|
Myocardial Stunning
|
Myoglobinuria, Acute Recurrent, Autosomal Recessive
|
Myopia
|
Myositis, Inclusion Body
|
Nasopharyngeal Neoplasm
|
Nbia2b
|
Neisseriaceae Infections
|
Neoplasm Recurrence, Local
|
Neoplasms, Experimental
|
Neoplasms, Second Primary
|
Nephritis
|
Nephroblastomatosis, Fetal Ascites, Macrosomia And Wilms Tumor
|
Nephrocalcinosis
|
Nephrotic Syndrome
|
Netherton Syndrome
|
Neural Tube Defect, Folate-Sensitive
|
Neuraminidase 1 Deficiency
|
Neuraminidase Deficiency With Beta-Galactosidase Deficiency
|
Neuroaxonal Dystrophies
|
Neuronopathy, Distal Hereditary Motor, Type V
|
Neutral Lipid Storage Disease With Myopathy
|
Neutropenia
|
Neutropenia, Severe Congenital, Autosomal Dominant 1
|
Neutropenia, Severe Congenital, Autosomal Recessive 4
|
Nevi And Melanomas
|
Nevus
|
Nevus, Epithelioid And Spindle Cell
|
Nicolaides Baraitser Syndrome
|
Niemann-Pick Diseases
|
Niemann-Pick Disease, Type A
|
Niemann-Pick Disease, Type B
|
Niemann-Pick Disease, Type C
|
Csnb1c
|
Night Blindness, Congenital Stationary, Autosomal Dominant 2
|
Nijmegen Breakage Syndrome-Like Disorder
|
Noonan Syndrome
|
Norman Roberts Lissencephaly Syndrome
|
Nose Neoplasms
|
Occipital Horn Syndrome
|
Oculocerebrorenal Syndrome
|
Oculopalatoskeletal Syndrome
|
Oligospermia
|
Ophthalmoplegia
|
Optic Atrophy
|
Optic Atrophy 1 And Deafness
|
Optic Atrophy, Autosomal Dominant
|
Optic Atrophy, Hereditary, Leber
|
Optic Neuritis
|
Orthomyxoviridae Infections
|
Ossification Of The Posterior Longitudinal Ligament Of The Spine
|
Osteochondrodysplasias
|
Osteochondroma
|
Osteolysis Hereditary Multicentric
|
Osteonecrosis
|
Osteosarcoma
|
Otofaciocervical Syndrome
|
Papillomavirus Infections
|
Papillon-Lefevre Disease
|
Paraganglioma
|
Paranoid Disorders
|
Paraplegia
|
Paratuberculosis
|
Parkinson Disease 7, Autosomal Recessive Early-Onset
|
Paroxysmal Nonkinesigenic Dyskinesia
|
Pemphigus, Benign Familial
|
Pericardial Effusion
|
Periodontal Diseases
|
Persian Gulf Syndrome
|
Pick Disease Of The Brain
|
Pigmentation Disorders
|
Pigmented Nodular Adrenocortical Disease, Primary, 2
|
Pilomatrixoma
|
Pituitary Acth Hypersecretion
|
Placenta Diseases
|
Plasminogen Deficiency, Type I
|
Pleuropulmonary Blastoma
|
Pneumonia, Viral
|
Poikiloderma With Neutropenia
|
Polycystic Kidney, Autosomal Recessive
|
Polycystic Kidney Diseases
|
Polycystic Liver Disease
|
Polydactyly
|
Polyneuropathies
|
Polyneuropathy, Hearing Loss, Ataxia, Retinitis Pigmentosa, And Cataract
|
Pontocerebellar Hypoplasia Type 1
|
Precursor T-Cell Lymphoblastic Leukemia-Lymphoma
|
Pregnancy Complications
|
Prekallikrein Deficiency
|
Prenatal Exposure Delayed Effects
|
Primary Dysautonomias
|
Primary Ovarian Insufficiency
|
Progeria
|
Progressive External Ophthalmoplegia With Mitochondrial Dna Deletions, Autosomal Dominant, 3
|
Prolidase Deficiency
|
Proprotein Convertase 1 3 Deficiency
|
Prostatic Intraepithelial Neoplasia
|
Protein C Deficiency
|
Proteus Syndrome
|
Pruritus
|
Psychoses, Substance-Induced
|
Purpura Fulminans
|
Purpura, Schoenlein-Henoch
|
Purpura, Thrombocytopenic, Idiopathic
|
Purpura, Thrombotic Thrombocytopenic
|
Pycnodysostosis
|
Pyruvate Dehydrogenase Phosphatase Deficiency
|
Rapadilino Syndrome
|
Respiratory Hypersensitivity
|
Respiratory Syncytial Virus Infections
|
Restless Legs Syndrome
|
Reticulocytosis
|
Retinal Cone Dystrophy 1
|
Retinal Cone Dystrophy 3a
|
Retinal Dystrophies
|
Retinitis Pigmentosa 33
|
Rett Syndrome
|
Rhabdoid Tumor Predisposition Syndrome 2
|
Rhabdomyosarcoma
|
Rhinitis
|
Rothmund-Thomson Syndrome
|
Sacral Defect And Anterior Sacral Meningocele
|
Sagittal Sinus Thrombosis
|
Salivary Gland Neoplasm
|
Sandhoff Disease
|
Sarcoma
|
Sarcopenia
|
Schimke Immunoosseous Dysplasia
|
Schindler Disease, Type I
|
Schizophrenia, Paranoid
|
Febrile Seizures
|
Seminoma
|
Sensory Ataxic Neuropathy, Dysarthria, And Ophthalmoparesis
|
Sertoli Cell-Only Syndrome
|
Severe Acute Respiratory Syndrome
|
Severe Combined Immunodeficiency, Autosomal Recessive, T Cell-Negative, B Cell-Negative, Nk Cell-Positive
|
Severe Combined Immunodeficiency, Autosomal Recessive, T Cell Negative, B Cell Positive, Nk Cell Positive
|
Severe Combined Immunodeficiency Due To Adenosine Deaminase Deficiency
|
Severe Combined Immunodeficiency With Sensitivity To Ionizing Radiation
|
Dengue Hemorrhagic Fever
|
Shock, Cardiogenic
|
N-Acetylneuraminic Acid Storage Disease
|
Sick Building Syndrome
|
Sinusitis
|
Sinus Thrombosis, Intracranial
|
Sjogren Syndrome
|
Skin Diseases, Vascular
|
Skin Ulcer
|
Sleep Apnea Syndromes
|
Spasms, Infantile
|
Spastic Paraplegia 39, Autosomal Recessive
|
Spastic Paraplegia 3, Autosomal Dominant
|
Spastic Paraplegia 4, Autosomal Dominant
|
Spastic Paraplegia 7, Autosomal Recessive
|
Spastic Paraplegia, Hereditary
|
Spherocytosis, Hereditary
|
Spinal Cord Compression
|
Spinal Cord Diseases
|
Spinal Cord Injuries
|
Spinal Dysraphism
|
Spinal Muscular Atrophy, Distal, X-Linked 3
|
Spinal Muscular Atrophy With Respiratory Distress 1
|
Spinocerebellar Ataxia 17
|
Spinocerebellar Ataxia 28
|
Spinocerebellar Ataxia, Autosomal Recessive 1
|
Spinocerebellar Ataxias
|
Ankylosing Spondylitis
|
Spondyloenchondrodysplasia
|
Spondyloepimetaphyseal Dysplasia, Missouri Type
|
Staphylococcal Infections
|
Stomach Ulcer
|
Striatal Degeneration, Autosomal Dominant
|
Subarachnoid Hemorrhage
|
Sunburn
|
Supratentorial Neoplasms
|
Tachycardia
|
Tay-Sachs Disease
|
Tay-Sachs Disease, Ab Variant
|
Testicular Diseases
|
Testicular Germ Cell Tumor
|
Thoracic Diseases
|
Thoracic Neoplasms
|
Thrombophilia, X-Linked, Due To Factor Ix Defect
|
Thrombotic Microangiopathies
|
Thyroid Carcinoma
|
Tight Skin Contracture Syndrome, Lethal
|
Tracheoesophageal Fistula
|
Trehalase Deficiency
|
Trismus
|
Hyperostosis-Hyperphosphatemia Syndrome
|
Turcot Syndrome
|
Tyrosinemias
|
Uridine 5-Prime Monophosphate Hydrolase Deficiency, Hemolytic Anemia Due To
|
Uterine Neoplasms
|
Uveal Melanoma
|
Vacterl Association With Hydrocephalus
|
Vasculopathy, Retinal, With Cerebral Leukodystrophy
|
Vasospasm, Intracranial
|
Vater Association
|
Ventricular Dysfunction
|
Ventricular Fibrillation
|
Vestibular Diseases
|
Vomiting
|
Wallerian Degeneration
|
Weight Loss
|
Weill-Marchesani Syndrome
|
Werner Syndrome
|
Woolly Hair, Congenital
|
Xeroderma Pigmentosum, Complementation Group B
|
Xeroderma Pigmentosum, Complementation Group D
|
Xeroderma Pigmentosum, Complementation Group F
|
Xeroderma Pigmentosum, Complementation Group G
|
Xfe Progeroid Syndrome
|
46,Xy Gonadal Dysgenesis, Complete Or Partial, Dhh-Related
|
Zimmerman Laband Syndrome
|
46,Xy Gonadal Dysgenesis, Partial, With Minifascicular Neuropathy
|
Abnormalities, Drug-Induced
|
Abruptio Placentae
|
Acrocapitofemoral Dysplasia
|
Acro-Osteolysis
|
Acth-Secreting Pituitary Adenoma
|
Acute-Phase Reaction
|
Adenoma, Liver Cell
|
Adenosine Monophosphate Deaminase Deficiency
|
Adjustment Disorders
|
Adrenocortical Carcinoma
|
Aggressive Periodontitis
|
Agricultural Workers' Diseases
|
Aicardi-Goutieres Syndrome 4
|
Aicardi-Goutieres Syndrome 5
|
Airway Obstruction
|
Alcohol Dependence
|
Androgenetic Alopecia
|
Alpha-Beta T-Cell Lymphopenia With Gamma-Delta T-Cell Expansion, Severe Cytomegalovirus Infection, And Autoimmunity
|
Alpha-Mannosidosis
|
Alpha-Thalassemia Myelodysplasia Syndrome
|
Alveolar Bone Loss
|
Alzheimer Disease, Familial, 3, With Spastic Paraparesis And Apraxia
|
Alzheimer Disease Type 4
|
Amaurosis Congenita Of Leber, Type 2
|
Amelogenesis Imperfecta, Hypomaturation Type, Iia2
|
Aminoacylase 1 Deficiency
|
Amnesia
|
Amnesia, Retrograde
|
Amyotrophic Lateral Sclerosis 11
|
Amyotrophic Lateral Sclerosis 4, Juvenile
|
Amyotrophic Lateral Sclerosis 9
|
Anaphylaxis
|
Anemia, Hemolytic
|
Anemia, Hemolytic, Congenital Nonspherocytic
|
Anemia, Hypoplastic, Congenital
|
Anemia, Iron-Deficiency
|
Sickle Cell Anemia
|
Angina Pectoris
|
Angina, Stable
|
Angioedemas, Hereditary
|
Angiokeratoma
|
Anisometropia
|
Antley-Bixler Syndrome Phenotype
|
Anuria
|
Anus, Imperforate
|
Aortic Aneurysm
|
Aphasia
|
Apnea
|
Cardiac Arrhythmia
|
Arterial Calcification Of Infancy
|
Arteriosclerosis
|
Asbestosis
|
Aspartylglucosaminuria
|
Asthenozoospermia
|
Ataxia
|
Atrial Fibrillation
|
Atrial Septal Defect 6
|
Atr-X Syndrome
|
Autoimmune Lymphoproliferative Syndrome
|
Autonomic Nervous System Diseases
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Azoospermia
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Azotemia
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Back Pain
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Bacteremia
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Bamforth Syndrome
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Bartter Syndrome
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Basal Ganglia Diseases
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Behcet's Syndrome
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Berylliosis
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Beta-Hydroxyisobutyryl Coa Deacylase Deficiency
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Beta-Thalassemia
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Beta-Ureidopropionase Deficiency
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Biotinidase Deficiency
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Blast Crisis
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Blindness
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Blister
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Blood Platelet Disorders
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Bone Diseases
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Bone Diseases, Metabolic
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Brachydactyly
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Brachydactyly Type A1
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Brachydactyly With Hypertension
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Brain Stem Neoplasms
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Branchio-Oto-Renal Syndrome
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Brody Myopathy
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Bronchial Hyperreactivity
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Bronchiectasis With Or Without Elevated Sweat Chloride 1
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Burkitt Lymphoma
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Burns, Chemical
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Butyrylcholinesterase Deficiency
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Cafe-Au-Lait Spots
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Calcification Of Joints And Arteries
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Canavan Disease
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Candidiasis, Oral
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Candidiasis, Vulvovaginal
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Capillary Malformation-Arteriovenous Malformation
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Carbon Tetrachloride Poisoning
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Carboxypeptidase N Deficiency
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Carcinoma, Mucoepidermoid
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Carcinoma, Pancreatic Ductal
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Carcinoma, Small Cell
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Cardiac Tamponade
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Cardiofaciocutaneous Syndrome
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Cardiomyopathies
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Cardiomyopathy, Dilated, 1j
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Cardiomyopathy, Dilated, 1u
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Cardiomyopathy, Dilated, 1v
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Cardiotoxicity
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Cardiovirus Infections
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Carnevale Syndrome
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Carotid Artery Diseases
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Carotid Artery Thrombosis
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Cataract
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Cayler Cardiofacial Syndrome
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Central Nervous System Neoplasms
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Cerebrooculofacioskeletal Syndrome 1
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Cerebrooculofacioskeletal Syndrome 2
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Cerebrooculofacioskeletal Syndrome 4
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Cerebrovascular Disorders
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Ceroid Lipofuscinosis, Neuronal, 1
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Ceroid Lipofuscinosis, Neuronal, 10
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Ceroid Lipofuscinosis, Neuronal, 2
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Charcot-Marie-Tooth Disease
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Charcot-Marie-Tooth Disease, Axonal, Type 2a2
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Charcot-Marie-Tooth Disease, Dominant Intermediate B
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Charcot-Marie-Tooth Disease, Type 2d
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Charcot-Marie-Tooth Disease, Type 4b1
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Charcot-Marie-Tooth Disease, Type 4j
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Charge Syndrome
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Chloracne
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Cholangitis
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Sclerosing Cholangitis
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Choledochal Cyst
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Choledocholithiasis
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Cholelithiasis
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Cholestasis
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Cholestasis, Intrahepatic
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Cholestasis, Progressive Familial Intrahepatic 3
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Cholesterol Ester Storage Disease
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Chordoma
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Chromosome 2q37 Deletion Syndrome
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Chromosome Breakage
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Ciliary Motility Disorders
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Cognitive Impairment
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Colorectal Adenomatous Polyposis, Autosomal Recessive
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Colorectal Neoplasms, Hereditary Nonpolyposis
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Color Vision Defects
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Combined Cellular And Humoral Immune Defects With Granulomas
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Complement Factor I Deficiency
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Cone Dystrophy 4
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Congenital Abnormalities
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Congenital Bilateral Aplasia Of Vas Deferens
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Congenital Cataracts, Facial Dysmorphism, And Neuropathy
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Congenital Disorder Of Glycosylation, Type Iib
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Congenital Thrombotic Disease, Due To Protein C Deficiency
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Connective Tissue Diseases
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Constipation
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Copper-Overload Cirrhosis
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Corneal Opacity
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Coronary Thrombosis
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Coronary Vasospasm
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Cortisone Reductase Deficiency
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Costello Syndrome
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Cough
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Coumarin Resistance
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Craniosynostosis Radial Aplasia Syndrome
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Crohn's Disease
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Cryopyrin-Associated Periodic Syndromes
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Currarino Triad
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Cyclic Neutropenia
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Cystic Fibrosis
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Darier Disease
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Deafness
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Deafness, Autosomal Dominant 10
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Deafness, Autosomal Recessive 12
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Death
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Death, Sudden
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Demyelinating Diseases
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Dent Disease 1
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Dent Disease 2
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Deoxyguanosine Kinase Deficiency
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Major Depression
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Dermatitis
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Dermatomyositis
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Desbuquois Syndrome
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Gestational Diabetes
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Diabetes Mellitus, Insulin-Dependent, 19
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Diabetes Mellitus, Noninsulin-Dependent, 1
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Diabetic Angiopathies
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Diarrhea
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Dihydropyrimidinase Deficiency
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Dimauro Disease
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Distal Myopathy, Nonaka Type
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Dna Repair-Deficiency Disorders
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Dog Diseases
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Down Syndrome
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Duodenal Ulcer
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Dysarthria
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Dyschromatosis Symmetrica Hereditaria 1
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Dyskinesia, Drug-Induced
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Dystonia 12
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Dystonia, Dopa-Responsive
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Dystonia Musculorum Deformans Type 1
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Dystonic Disorders
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Early-Onset Ataxia With Oculomotor Apraxia And Hypoalbuminemia
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Ehlers-Danlos Syndrome, Type Vii, Autosomal Recessive
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Emaciation
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Embolism
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Embolism And Thrombosis
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Embryo Loss
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Emphysema
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Encephalomyelitis, Autoimmune, Experimental
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Enchondromatosis
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Endocrine System Diseases
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Endotoxemia
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End Stage Liver Disease
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Enterokinase Deficiency
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Epilepsy, Tonic-Clonic
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Erythema Multiforme
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Esophageal Squamous Cell Carcinoma
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Esophagitis
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Exocrine Pancreatic Insufficiency
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Exostoses, Multiple Hereditary
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Fabry Disease
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Factor Vii Deficiency
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Factor X Deficiency
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Factor Xi Deficiency
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Factor Xii Deficiency
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Familial Cylindromatosis
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Familial Hypophosphatemic Rickets
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Fanconi Anemia, Complementation Group J
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Farber Lipogranulomatosis
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Fasciculation
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Fetal Diseases
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Fetal Growth Retardation
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Fever
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Flushing
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Frontotemporal Dementia
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Fructose-1,6-Diphosphatase Deficiency
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Fucosidosis
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Gallbladder Neoplasm
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Gangliosidosis, Gm1
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Gastrointestinal Diseases
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Gastrointestinal Hemorrhage
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Gaucher Disease, Perinatal Lethal
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Gaucher Disease, Type Iiic
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Genomic Instability
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Glaucoma, Angle-Closure
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Gliosarcoma
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Glomerulonephritis
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Glomerulonephritis, Membranoproliferative
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Membranous Glomerulonephritis
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Focal Segmental Glomerulosclerosis
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Glutathionuria
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Glycogen Storage Disease Type I
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Glycogen Storage Disease Type Ii
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Glycogen Storage Disease Type V
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Graft Occlusion, Vascular
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Wegener's Granulomatosis
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Hair Diseases
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Hamartoma Syndrome, Multiple
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Head And Neck Neoplasms
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Hearing Loss, Conductive
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Noise-Induced Hearing Loss
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Heart Rupture, Post-Infarction
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Heart Septal Defects
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Heart Septal Defects, Ventricular
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Heat Stroke
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Helicobacter Infections
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Hemangioma
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Hematologic Neoplasms
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Hematoma, Epidural, Spinal
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Hematoma, Subdural
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Hematoma, Subdural, Acute
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Hemiplegic Migraine, Familial Type 2
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Hemolysis
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Hemophilia A
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Hemophilia B
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Hemorrhagic Disorders
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Hemorrhoids
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Hepatomegaly
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Hepatorenal Form Of Glycogen Storage Disease
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Hereditary Angioedema Type Iii
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Hereditary Autoinflammatory Diseases
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Hereditary Motor And Sensory Neuropathy Vi
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Hernia, Umbilical
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Heterotaxy Syndrome
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Hidradenitis Suppurativa, Familial
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Hirschsprung Disease
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Histiocytoma, Benign Fibrous
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Hiv-Associated Lipodystrophy Syndrome
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Homocarnosinosis
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Hyaluronidase Deficiency
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Hydroxykynureninuria
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Hyperaldosteronism
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Hyperargininemia
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Hypercalcemia
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Hypercalcemia, Idiopathic, Of Infancy
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Hypercalciuria, Childhood Idiopathic
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Hypercholanemia, Familial
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Hypercholesterolemia, Autosomal Dominant, 3
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Hyperinsulinism
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Hyperkeratosis, Epidermolytic
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Hyperkinesis
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Hyperlipidemia, Combined, 2
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Hyperlipoproteinemia Type I
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Hypermethioninemia
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Hyperphenylalaninemia, Bh4-Deficient, B
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Hyperphosphatemia
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Allergy
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Hypersensitivity, Immediate
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Hypertension, Essential
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Hypertension, Malignant
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Hyperthyroidism
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Hyperuricemic Nephropathy, Familial Juvenile 2
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Hypogonadism
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Hypokinesia
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Hypophosphatasia, Adult
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Hypophosphatasia, Childhood
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Hypophosphatasia, Infantile
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Hypophosphatemic Rickets, Autosomal Recessive, 2
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Hypoprothrombinemias
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Hypotrichosis
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Ichthyosis Follicularis Atrichia Photophobia Syndrome
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Ichthyosis With Hypotrichosis, Autosomal Recessive
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Ichthyosis, X-Linked
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Idiopathic Hypogonadotropic Hypogonadism
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Iga Deficiency
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Ige Responsiveness, Atopic
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Immune Complex Diseases
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Immune System Disease
|
Immunologic Deficiency Syndromes
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Inclusion Body Myopathy Autosomal Recessive
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Inclusion Body Myopathy With Early-Onset Paget Disease And Frontotemporal Dementia
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Infant, Premature, Diseases
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Infection
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Infertility
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Infertility, Female
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Inherited Peripheral Neuropathy
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