Liver Cirrhosis, Experimental
|
Breast Carcinoma
|
Prostatic Neoplasms
|
Hepatocellular Carcinoma
|
Lung Neoplasms
|
Autism
|
Craniofacial Abnormalities
|
Hypertension
|
Stomach Neoplasms
|
Colorectal Cancer
|
Colonic Neoplasm
|
Drug-Induced Liver Injury
|
Diabetes Mellitus, Type 2
|
Rheumatoid Arthritis
|
Myocardial Ischemia
|
Carcinoma
|
Heart Failure
|
Diabetes Mellitus, Experimental
|
Schizophrenia
|
Obesity
|
Seizures
|
Endometriosis
|
Squamous Cell Carcinoma
|
Mammary Neoplasms, Experimental
|
Leukemia, Myeloid, Acute
|
Neoplasm Metastasis
|
Neoplasm Invasiveness
|
Melanoma
|
Carcinoma, Non-Small-Cell Lung
|
Acute Kidney Injury
|
Mammary Neoplasms, Animal
|
Glioma
|
Renal Cell Carcinoma
|
Adenocarcinoma
|
Reperfusion Injury
|
Kidney Failure, Chronic
|
Disease Progression
|
Inflammation
|
Cell Transformation, Neoplastic
|
Neurodegenerative Diseases
|
Status Epilepticus
|
Asthma
|
Myocardial Infarction
|
Atherosclerosis
|
Polycystic Ovary Syndrome
|
Cocaine Dependence
|
Parkinson's Disease
|
Nerve Degeneration
|
Alzheimer's Disease
|
Nervous System Diseases
|
Dermatitis, Contact
|
Ovarian Neoplasms
|
Drug-Related Side Effects And Adverse Reactions
|
Amphetamine-Related Disorders
|
Esophageal Neoplasms
|
Pulmonary Fibrosis
|
Lung Diseases
|
Abortion, Spontaneous
|
Skin Neoplasms
|
Hiv Infections
|
Liver Diseases
|
Neoplasms
|
Brain Ischemia
|
Pancreatic Carcinoma
|
Liver Cirrhosis
|
Kidney Disease
|
Bipolar Disorder
|
Mesothelioma, Malignant
|
Diabetic Nephropathy
|
Urinary Bladder Neoplasms
|
Mouth Neoplasms
|
Leukemia, Promyelocytic, Acute
|
Osteoporosis
|
Liver Neoplasms
|
Drug Dependence
|
Unipolar Depression
|
Systemic Lupus Erythematosus
|
Intellectual Disability
|
Psoriasis
|
Proteinuria
|
Hernia, Diaphragmatic
|
Memory Disorders
|
Cardiovascular Disease
|
Osteoarthritis
|
Non-Alcoholic Fatty Liver Disease
|
Precancerous Conditions
|
Fatty Liver
|
Coronary Artery Disease
|
Glioblastoma Multiforme
|
Thrombosis
|
Esophageal Squamous Cell Carcinoma
|
Cognitive Impairment
|
Myocardial Reperfusion Injury
|
Substance Withdrawal Syndrome
|
Heart Defects, Congenital
|
Weight Gain
|
Arthritis, Juvenile
|
Hypotension
|
Parkinsonian Disorders
|
Diabetes Mellitus
|
Acute Lymphoblastic Leukemia
|
Diabetes Mellitus, Type 1
|
Fibrosis
|
Liver Neoplasms, Experimental
|
Epilepsy
|
Insulin Resistance
|
Intracerebral Hemorrhage
|
Keloid
|
Malaria
|
Hyperalgesia
|
Lymphoma, Non-Hodgkin
|
Thyroid Carcinoma
|
Cardiomyopathies
|
Hepatitis, Chronic
|
Brain Injuries
|
Neuroblastoma
|
Ulcerative Colitis
|
Male Infertility
|
Cholangiocarcinoma
|
Dilated Cardiomyopathy
|
Small Cell Lung Carcinoma
|
Astrocytoma
|
Retinal Diseases
|
Intestinal Neoplasms
|
Autism Spectrum Disorder
|
Allergy
|
Atrial Fibrillation
|
Respiratory Distress Syndrome, Adult
|
Infarction, Middle Cerebral Artery
|
Adenoma
|
Primary Biliary Cirrhosis
|
Alcoholic Liver Cirrhosis
|
Anemia, Hemolytic
|
Amyotrophic Lateral Sclerosis
|
Leukemia-Lymphoma, Adult T-Cell
|
Arthritis, Experimental
|
Calcinosis
|
Head And Neck Neoplasms
|
Heart Diseases
|
Heat Stroke
|
Necrosis
|
Neoplasm Recurrence, Local
|
Stroke
|
Crohn's Disease
|
Spinal Dysraphism
|
Learning Disorders
|
Acute Coronary Syndrome
|
Skin Diseases
|
Colitis
|
Ischemia
|
Autoimmune Disease
|
Mesothelioma
|
Hyperkinesis
|
Enterocolitis, Necrotizing
|
Oligodendroglioma
|
Ventricular Remodeling
|
Lymphoma, Large B-Cell, Diffuse
|
Hemolysis
|
Stomach Ulcer
|
Neoplasms, Experimental
|
Leukemia
|
Endometrial Neoplasm
|
Psoriatic Arthritis
|
Brain Diseases
|
Marfan Syndrome
|
Chronic Lymphocytic Leukemia
|
Amyotrophic Lateral Sclerosis 1
|
Growth Disorders
|
Dermatitis, Allergic Contact
|
Muscular Diseases
|
Eye Abnormalities
|
Osteosarcoma
|
Copper-Overload Cirrhosis
|
Weight Loss
|
Cholestasis
|
Acute Lung Injury
|
Pain
|
Tooth Abnormalities
|
Tuberculosis
|
Uterine Cervical Neoplasms
|
Bone Diseases, Developmental
|
Focal Segmental Glomerulosclerosis
|
Chronic Obstructive Pulmonary Disease
|
Pulmonary Embolism
|
Hypercholesterolemia
|
Disease Models, Animal
|
Iga Glomerulonephritis
|
Hyperplasia
|
Hyperemia
|
Cardiac Hypertrophy
|
Dyskinesia, Drug-Induced
|
Diabetic Retinopathy
|
Lung Adenocarcinoma
|
Hyperthyroidism
|
Anemia
|
Pulmonary Hypertension
|
Retinal Degeneration
|
Hypercholesterolemia, Familial
|
Pneumonia
|
Carcinoma, Pancreatic Ductal
|
Hepatolenticular Degeneration
|
Medulloblastoma
|
Vasospasm, Intracranial
|
Epilepsy, Temporal Lobe
|
Skin Abnormalities
|
Aortic Aneurysm
|
Age-Related Macular Degeneration
|
Gallbladder Neoplasm
|
Chromosome Aberrations
|
Brain Neoplasms
|
Cleft Lip
|
Genetic Predisposition To Disease
|
Metabolic Syndrome X
|
Microsatellite Instability
|
Amino Acid Metabolism, Inborn Errors
|
Cardiac Arrhythmia
|
Arsenic Poisoning
|
Multiple Sclerosis
|
Muscular Atrophy
|
Coronary Heart Disease
|
Hearing Loss
|
Craniosynostoses
|
Nasopharyngeal Carcinoma
|
Carcinoma, Adenoid Cystic
|
Nephrotic Syndrome
|
Basal Cell Carcinoma
|
Neuroectodermal Tumors, Primitive
|
Asbestosis
|
Neurotoxicity Syndromes
|
Asphyxia Neonatorum
|
Occupational Diseases
|
Carcinoma, Small Cell
|
Carcinoma, Transitional Cell
|
Adenocarcinoma Of Esophagus
|
Huntington Disease
|
Osteitis Deformans
|
Major Depression
|
Osteochondrodysplasias
|
Atopic Eczema
|
Ovarian Cysts
|
Asthma, Occupational
|
Papilloma
|
Hyperglycemia
|
Peripheral Neuropathy
|
Hyperhomocysteinemia
|
Hyperlipidemias
|
Diabetic Angiopathies
|
Pheochromocytoma
|
Hypertension, Essential
|
Cardiomyopathy, Familial Hypertrophic, 1
|
Down Syndrome
|
Attention Deficit Hyperactivity Disorder
|
Hypothermia
|
Protein Deficiency
|
Hypoxia-Ischemia, Brain
|
Psychosis
|
Duodenal Ulcer
|
Cardiomyopathy, Hypertrophic
|
Cardiomyopathy, Hypertrophic, Familial
|
Cardiovascular Abnormalities
|
Limb Dystonia
|
Infertility, Female
|
Inflammatory Bowel Disease
|
Influenza, Human
|
Cone-Rod Dystrophy 2
|
Edema
|
Albuminuria
|
Juvenile Polyposis Syndrome
|
Emphysema
|
Barrett's Esophagus
|
Kidney Neoplasms
|
Berylliosis
|
Spinal Cord Injuries
|
Visceral Leishmaniasis
|
Ankylosing Spondylitis
|
Leukemia, Lymphoid
|
Leukemia, Myeloid
|
Tetralogy Of Fallot
|
Thrombocythemia, Essential
|
Leukoencephalopathies
|
Adrenocortical Carcinoma
|
Tongue Neoplasms
|
Limb Deformities, Congenital
|
Bone Diseases
|
Turner Syndrome
|
Ureteral Calculi
|
Furlong Syndrome
|
Ventricular Dysfunction, Left
|
Long Qt Syndrome
|
Anxiety Disorder
|
Chloracne
|
Lymphangioleiomyomatosis
|
Fever
|
Phencyclidine Abuse
|
Dystonic Disorders
|
Intestinal Polyps
|
Pfeiffer Type Acrocephalosyndactyly
|
Salivary Gland Neoplasm
|
Pasteurellaceae Infections
|
Sarcoidosis
|
Mental Disorders
|
Anemia, Iron-Deficiency
|
Iron Metabolism Disorders
|
Parkinson Disease, Secondary
|
Gastrointestinal Stromal Tumors
|
Schistosomiasis Mansoni
|
Diabetes Complications
|
Jackson-Weiss Syndrome
|
Alcohol Dependence
|
Scrapie
|
Vascular Diseases
|
Developmental Disabilities
|
Vascular System Injuries
|
Sepsis
|
Bare Lymphocyte Syndrome, Type I
|
Osteoporosis, Postmenopausal
|
Organophosphate Poisoning
|
Sexual Dysfunctions, Psychological
|
Oral Submucous Fibrosis
|
Kidney Stone
|
Hodgkins Lymphoma
|
Aortic Diseases
|
Hirschsprung Disease
|
Gastroesophageal Reflux
|
Basal Ganglia Diseases
|
Aneurysm, Dissecting
|
Lymphoma, Follicular
|
Kyphosis
|
Carcinoma, Squamous Cell Of Head And Neck
|
Language Development Disorders
|
Heroin Dependence
|
Deafness
|
Csnb1c
|
Neutropenia
|
Acromicric Dysplasia
|
Hepatitis, Autoimmune
|
Spasms, Infantile
|
Neuroendocrine Tumors
|
Carcinoma, Ductal, Breast
|
Uterine Fibroid
|
Beta-Thalassemia
|
Thoracic Aortic Aneurysm
|
Neurobehavioral Manifestations
|
Hepatitis
|
Mastocytosis, Systemic
|
Erectile Dysfunction
|
Splenomegaly
|
Lymphoma, Large-Cell, Anaplastic
|
Neuropathic Pain
|
Hepatic Encephalopathy
|
Hemochromatosis
|
Toxic Epidermal Necrolysis
|
Lethargy
|
Neoplasms, Second Primary
|
Acrocephalosyndactylia
|
Neoplasms, Germ Cell And Embryonal
|
Hemangiosarcoma
|
Heart Valve Diseases
|
Hamartoma Syndrome, Multiple
|
Myeloproliferative Disorder
|
Chilblain Lupus 1
|
Sudden Infant Death
|
Mycobacterium Infections, Nontuberculous
|
Coronary Restenosis
|
Exostoses, Multiple Hereditary
|
Syndactyly
|
Chronic Myelogenous Leukemia
|
Tachycardia
|
Marijuana Dependence
|
Musculoskeletal Abnormalities
|
Cardiomyopathy, Dilated, 3b
|
Testicular Germ Cell Tumor
|
Arteriosclerosis
|
Bone Neoplasms
|
Lung Injury
|
Burns
|
Amyloidosis
|
Manganese Poisoning
|
Multiple Myeloma
|
Glycogen Storage Disease Type V
|
Lewy Body Dementia
|
Chondrosarcoma, Mesenchymal
|
Familial Testotoxicosis
|
Thyroid Hormone Resistance Syndrome
|
Anoxia
|
Movement Disorder
|
Nicotine Dependence
|
Brain Edema
|
Mouth Diseases
|
Adrenoleukodystrophy
|
Aortic Valve Insufficiency
|
Tremor
|
Motor Skills Disorders
|
Lipidoses
|
Congenital Central Hypoventilation Syndrome
|
Zellweger Syndrome
|
Morphine Dependence
|
Lymphatic Metastasis
|
Uremia
|
Lymphoma, T-Cell, Cutaneous
|
Ureteral Obstruction
|
Glucose Intolerance
|
Migraine Without Aura
|
Migraine Disorder
|
Psychoses, Substance-Induced
|
Pulmonary Edema
|
Prolactinoma
|
Pulmonary Emphysema
|
Drug Hypersensitivity
|
Hypokalemia
|
Breast Neoplasms, Male
|
Idiopathic Pulmonary Fibrosis
|
Colorectal Neoplasms, Hereditary Nonpolyposis
|
Radiation Injuries, Experimental
|
Urologic Neoplasms
|
Rectum Cancer
|
Recurrence
|
Urticaria
|
Premature Birth
|
Hypoglycemia
|
Renal Insufficiency
|
Chronic Kidney Disease
|
Dyslipidemias
|
Preeclampsia
|
Left Ventricular Hypertrophy
|
Precursor B-Cell Lymphoblastic Leukemia-Lymphoma
|
Micronuclei, Chromosome-Defective
|
Respiratory System Abnormalities
|
Liver Diseases, Parasitic
|
Polycystic Kidney, Autosomal Dominant
|
Poisoning
|
Abnormalities, Multiple
|
Atrial Fibrillation, Familial, 3
|
Fetal Alcohol Spectrum Disorders
|
Pleural Diseases
|
Hyperoxaluria
|
Open-Angle Glaucoma
|
Diabetic Neuropathies
|
Hyperphenylalaninemia, Bh4-Deficient, C
|
Rhabdomyosarcoma
|
Carotid Artery Diseases
|
Myositis
|
Myositis Ossificans
|
Myostatin-Related Muscle Hypertrophy
|
Myotonia Congenita
|
Myotonic Dystrophy
|
Nasopharyngeal Neoplasm
|
Naxos Disease
|
Neoplasms, Radiation-Induced
|
Neoplasms, Squamous Cell
|
Neovascularization, Pathologic
|
Nephritis
|
Alport Syndrome, X-Linked
|
Nephritis, Interstitial
|
Nephrosis
|
Neural Tube Defects
|
Neuroaxonal Dystrophies
|
Neuroectodermal Tumors, Primitive, Peripheral
|
Neurofibromatosis 1
|
Neurogenic Inflammation
|
Neurologic Manifestations
|
Neuronal Ceroid-Lipofuscinoses
|
Nevo Syndrome
|
Night Blindness, Congenital Stationary, Autosomal Dominant 1
|
Multiple Synostoses Syndrome 1
|
No-Reflow Phenomenon
|
Norrie Disease
|
Nystagmus, Congenital
|
Obesity, Morbid
|
Obsessive-Compulsive Disorder
|
Ocular Hypertension
|
Oculocutaneous Albinism Type 1
|
Oculocutaneous Albinism Type 1b
|
Oculocutaneous Albinism Type 3
|
Oculopalatoskeletal Syndrome
|
Ophthalmoplegia, Chronic Progressive External
|
Hypertelorism With Esophageal Abnormality And Hypospadias
|
Opitz-Kaveggia Syndrome
|
Optic Atrophy
|
Optic Atrophy Polyneuropathy Deafness
|
Orofacial Cleft 11
|
Ossification Of The Posterior Longitudinal Ligament Of The Spine
|
Osteoarthropathy, Primary Hypertrophic
|
Osteoglophonic Dwarfism
|
Oto-Palato-Digital Syndrome Type 1
|
Oto-Palato-Digital Syndrome, Type 2
|
Pancreatic Diseases
|
Pancreatitis
|
Panic Disorder
|
Paratuberculosis
|
Parkinson Disease 7, Autosomal Recessive Early-Onset
|
Cousin Syndrome
|
Penile Induration
|
Pericardial Effusion
|
Periodontitis
|
Peripheral Arterial Disease
|
Peripheral Vascular Diseases
|
Peritoneal Fibrosis
|
Heterotopia, Periventricular, Ehlers-Danlos Variant
|
Peroxisomal Disorders
|
Persian Gulf Syndrome
|
Personality Disorders
|
Peters Anomaly
|
Phagocyte Bactericidal Dysfunction
|
Pharyngeal Neoplasms
|
Phobic Disorders
|
Phosphoribosylpyrophosphate Synthetase Superactivity
|
Photophobia
|
Phyllodes Tumor
|
Piebaldism
|
Pigmentation Disorders
|
Pituitary Neoplasms
|
Plagiocephaly, Nonsynostotic
|
Plaque, Amyloid
|
Plaque, Atherosclerotic
|
Platelet Disorder, Familial, With Associated Myeloid Malignancy
|
Pneumococcal Infections
|
Pneumonia, Aspiration
|
Pneumonia, Viral
|
Polymorphic Catecholergic Ventricular Tachycardia
|
Polyneuropathies
|
Polyposis Syndrome, Hereditary Mixed, 2
|
Porphyria Cutanea Tarda
|
Precursor T-Cell Lymphoblastic Leukemia-Lymphoma
|
Pregnancy Complications
|
Prekallikrein Deficiency
|
Prenatal Injuries
|
Primary Hyperoxaluria Type 1
|
Primary Hyperoxaluria Type 2
|
Primary Lateral Sclerosis Juvenile
|
Primary Ovarian Insufficiency
|
Primary Ovarian Insufficiency, Fragile X-Associated
|
Prostate Cancer, Familial
|
Prostate Cancer, Hereditary, 11
|
Pseudohypoaldosteronism
|
Psychomotor Disorders
|
Puberty, Precocious
|
Purine-Pyrimidine Metabolism, Inborn Errors
|
Pyloric Stenosis, Infantile Hypertrophic 1
|
Pyruvate Dehydrogenase Phosphatase Deficiency
|
Q Fever
|
Raynaud Disease
|
Reflex, Abnormal
|
Refsum Disease
|
Renal Cysts And Diabetes Syndrome
|
Renal Tubular Acidosis, Distal, Autosomal Recessive
|
Renal Tubular Acidosis, Distal, With Hemolytic Anemia
|
Respiratory Insufficiency
|
Respiratory Tract Diseases
|
Respiratory Tract Infections
|
Reticulocytosis
|
Reticuloendotheliosis, Familial, With Eosinophilia
|
Retinal Detachment
|
Retinal Vein Occlusion
|
Retinitis Pigmentosa 4
|
Retinitis Pigmentosa 42
|
Rhizomelic Chondrodysplasia Punctata, Type 1
|
Ring Dermoid Of Cornea
|
Romano-Ward Syndrome
|
Rosselli-Gulienetti Syndrome
|
Saethre-Chotzen Syndrome With Eyelid Anomalies
|
Sandhoff Disease
|
Sarcoma, Synovial
|
Sarcopenia
|
Scaphocephaly, Maxillary Retrusion, And Mental Retardation
|
Schindler Disease, Type I
|
Schistosomiasis
|
Systemic Scleroderma
|
Scott Syndrome
|
Sea-Blue Histiocyte Syndrome
|
Febrile Seizures
|
Severe Acute Respiratory Syndrome
|
Severe Combined Immunodeficiency
|
Severe Combined Immunodeficiency, Autosomal Recessive, T Cell-Negative, B Cell-Negative, Nk Cell-Positive
|
Sezary Syndrome
|
Septic Shock
|
Short Qt Syndrome 1
|
Short Qt Syndrome 2
|
Short Stature, Idiopathic, Autosomal
|
Shprintzen Golberg Craniosynostosis
|
Sick Sinus Syndrome
|
Silicosis
|
Silver-Russell Syndrome
|
Sinusitis
|
Situs Inversus
|
Skeletal Defects, Genital Hypoplasia, And Mental Retardation
|
Sleep Disorders, Circadian Rhythm
|
Soft Tissue Neoplasms
|
Specific Granule Deficiency
|
Spherocytosis, Hereditary
|
Spherocytosis, Type 4
|
Spina Bifida Cystica
|
Spinal Muscular Atrophy, Late-Onset, Finkel Type
|
Spinocerebellar Ataxia 17
|
Spinocerebellar Ataxia, Autosomal Recessive 8
|
Spondylocheirodysplasia, Ehlers-Danlos Syndrome-Like
|
Staphylococcal Infections
|
Stomach Diseases
|
Subarachnoid Hemorrhage
|
Succinic Semialdehyde Dehydrogenase Deficiency
|
Succinyl-Coa:3-Oxoacid Coa Transferase Deficiency
|
Progressive Supranuclear Palsy
|
Surfactant Metabolism Dysfunction, Pulmonary, 1
|
Surfactant Metabolism Dysfunction, Pulmonary, 2
|
Syndactyly Cenani Lenz Type
|
Tachycardia, Ventricular
|
Takayasu Arteritis
|
Telangiectasia, Hereditary Hemorrhagic
|
Testicular Neoplasms
|
Thrombocytopenia
|
Thrombotic Microangiopathies
|
Thyroid Cancer, Papillary
|
Thyroid Dyshormonogenesis 3
|
Thyroid Hormone Resistance, Generalized, Autosomal Dominant
|
Thyroid Hormone Resistance, Generalized, Autosomal Recessive
|
Thyroid Hormone Resistance, Selective Pituitary
|
Thyroiditis, Autoimmune
|
Torsades De Pointes
|
Trauma, Nervous System
|
Tuberous Sclerosis
|
Tuberous Sclerosis 1
|
Tuberous Sclerosis 2
|
Turcot Syndrome
|
Urinary Bladder Neck Obstruction
|
Urinary Tract Infections
|
Urination Disorders
|
Urogenital Abnormalities
|
Usher Syndromes
|
Usher Syndrome, Type 1b
|
Usher Syndrome, Type 2a
|
Usher Syndrome, Type Ig
|
Uterine Neoplasms
|
Uveitis
|
Vasculopathy, Retinal, With Cerebral Leukodystrophy
|
Ventricular Fibrillation
|
Vesicoureteral Reflux 2
|
Vestibular Diseases
|
Vision Disorders
|
Vitamin A Deficiency
|
Von Willebrand Disease, Type 1
|
Von Willebrand Disease, Type 2
|
Von Willebrand Disease, Type 3
|
Werner Syndrome
|
Wernicke Encephalopathy
|
Wolcott-Rallison Syndrome
|
Wolfram Syndrome 2
|
Wounds And Injuries
|
Xanthinuria, Type I
|
Xeroderma Pigmentosum
|
Xeroderma Pigmentosum, Complementation Group G
|
3-Hydroxy-3-Methylglutaryl-Coa Lyase Deficiency
|
Zlotogora-Ogur Syndrome
|
46, Xx Disorders Of Sex Development
|
46, Xy Disorders Of Sex Development
|
6-Pyruvoyl-Tetrahydropterin Synthase Deficiency
|
Abnormalities, Drug-Induced
|
Acatalasia
|
Acidosis, Lactic
|
Acidosis, Renal Tubular
|
Acth-Secreting Pituitary Adenoma
|
Acute-Phase Reaction
|
Adenocarcinoma, Clear Cell
|
Adenocarcinoma, Follicular
|
Adenoma, Liver Cell
|
Adenoma, Oxyphilic
|
Adenomatous Polyposis Coli
|
Adrenal Gland Neoplasms
|
Aging, Premature
|
Agricultural Workers' Diseases
|
Aicardi-Goutieres Syndrome
|
Aids-Related Kaposi Sarcoma
|
Aids-Related Opportunistic Infections
|
Albinism Ocular Late Onset Sensorineural Deafness
|
Albinism, Oculocutaneous
|
Albinism With Hemorrhagic Diathesis And Pigmented Reticuloendothelial Cells
|
Allanson Pantzar Mcleod Syndrome
|
Androgenetic Alopecia
|
Alopecia Areata
|
Alpha-B Crystallinopathy
|
Alpha-Beta T-Cell Lymphopenia With Gamma-Delta T-Cell Expansion, Severe Cytomegalovirus Infection, And Autoimmunity
|
Alveolar Capillary Dysplasia
|
Alzheimer Disease Type 2
|
Amyotrophic Lateral Sclerosis 2, Juvenile
|
Amyotrophic Lateral Sclerosis 8
|
Amyotrophic Lateral Sclerosis 9
|
Anemia, Aplastic
|
Anemia, Diamond-Blackfan
|
Anemia, Hemolytic, Congenital Nonspherocytic
|
Anemia, Megaloblastic
|
Sickle Cell Anemia
|
Angiokeratoma
|
Ankylosis
|
Anophthalmia With Pulmonary Hypoplasia
|
Anophthalmos
|
Anti-Plasmin Deficiency, Congenital
|
Antley-Bixler Syndrome Phenotype
|
Apraxias
|
Arachnodactyly
|
Arenaviridae Infections
|
Arrhythmogenic Right Ventricular Dysplasia, Familial, 12
|
Arterial Calcification Of Infancy
|
Arteritis
|
Arthritis
|
Arts Syndrome
|
Asperger Syndrome
|
Aspirin Induced Asthma
|
Atrial Fibrillation, Familial, 4
|
Atrophy
|
Attention Deficit And Disruptive Behavior Disorders
|
Atypical Mycobacteriosis, Familial, X-Linked 1
|
Auditory Perceptual Disorders
|
Autonomic Nervous System Diseases
|
Azoospermia
|
Bacteremia
|
Behcet's Syndrome
|
Beta Ketothiolase Deficiency
|
Birk-Barel Mental Retardation Dysmorphism Syndrome
|
Birth Weight
|
Blood Coagulation Disorders
|
Blue Cone Monochromatism
|
Body Weight
|
Bone Diseases, Endocrine
|
Bone Diseases, Metabolic
|
Bowen's Disease
|
Brachydactyly
|
Bradycardia
|
Brain Diseases, Metabolic
|
Branchio-Oto-Renal Syndrome
|
Brody Myopathy
|
Bronchial Diseases
|
Chronic Bronchitis
|
Brugada Syndrome
|
Brugada Syndrome 2
|
Burkitt Lymphoma
|
Burns, Chemical
|
Buruli Ulcer
|
Cachexia
|
Cafe Au Lait Spots, Multiple
|
Camurati-Engelmann Syndrome
|
Candidiasis, Chronic Mucocutaneous
|
Carbon Tetrachloride Poisoning
|
Carcinogenesis
|
Carcinoma In Situ
|
Carcinoma, Large Cell
|
Carcinoma, Lewis Lung
|
Carcinoma, Medullary
|
Carcinosarcoma
|
Cardiac Valvular Dysplasia, X-Linked
|
Cardiomyopathy, Dilated, 1aa
|
Cardiomyopathy, Dilated, 1ee
|
Cardiomyopathy, Dilated, 1s
|
Cardiomyopathy, Dilated, 1w
|
Cardiomyopathy, Dilated, 1y
|
Cardiomyopathy, Dilated, 1z
|
Cardiomyopathy, Familial Hypertrophic, 13
|
Cardiomyopathy, Familial Hypertrophic, 14
|
Cardiomyopathy, Familial Hypertrophic, 15
|
Cardiomyopathy, Familial Hypertrophic, 3
|
Carnevale Syndrome
|
Carotid Artery Thrombosis
|
Carotid Stenosis
|
Cartilage Diseases
|
Catalepsy
|
Cataract
|
Cataract, Congenital Zonular, With Sutural Opacities
|
Cataract, Coppock-Like
|
Cataract, Posterior Polar, 3
|
Cataract, Pulverulent, Juvenile-Onset
|
Caudal Duplication Anomaly
|
Cd8 Deficiency, Familial
|
Cerebellar Diseases
|
Cerebral Amyloid Angiopathy
|
Cerebral Cavernous Malformations 3
|
Cerebral Infarction
|
Cerebrooculofacioskeletal Syndrome 1
|
Ceroid Lipofuscinosis, Neuronal, 6
|
Cerulean Cataract
|
Charcot-Marie-Tooth Disease, Type 4b1
|
Charcot-Marie-Tooth Disease, Type 4b2
|
Charcot-Marie-Tooth Disease, X-Linked, 1
|
Char Syndrome
|
Cholangitis
|
Sclerosing Cholangitis
|
Cholestasis, Intrahepatic
|
Chondrodysplasia Punctata, Rhizomelic
|
Chondroma
|
Chondrosarcoma
|
Chondrosarcoma, Extraskeletal Myxoid
|
Choroidal Neovascularization
|
Chromosome Breakage
|
Classical Lissencephalies And Subcortical Band Heterotopias
|
Clear-Cell Metastatic Renal Cell Carcinoma
|
Coloboma
|
Color Vision Defects
|
Combined Cellular And Humoral Immune Defects With Granulomas
|
Congenital Abnormalities
|
Congenital Disorder Of Glycosylation Type 2d
|
Congenital Idiopathic Intestinal Pseudoobstruction
|
Connective Tissue Diseases
|
Constipation
|
Coproporphyria, Hereditary
|
Corneal Neovascularization
|
Coronary Artery Disease, Autosomal Dominant 2
|
Coronary Stenosis
|
Coronary Vasospasm
|
Cough
|
Craniofacial Dysostosis
|
Creutzfeldt Jacob Disease
|
Cri-Du-Chat Syndrome
|
Crigler-Najjar Syndrome
|
Crigler Najjar Syndrome, Type 2
|
Cushing's Symphalangism
|
Cutis Gyrata Syndrome Of Beare And Stevenson
|
Cutis Laxa, Recessive
|
Cyanosis
|
Cystic Fibrosis
|
Cystitis
|
Cytomegalovirus Infection
|
Deafness, Autosomal Dominant 11
|
Deafness, Autosomal Dominant Nonsyndromic Sensorineural 17
|
Deafness, Autosomal Recessive 2
|
Deafness, Autosomal Recessive, 24
|
Deafness, Autosomal Recessive 31
|
Deafness, X-Linked 1
|
Death, Sudden
|
Deficiency Diseases
|
Demyelinating Diseases
|
Desbuquois Syndrome
|
Gestational Diabetes
|
Diabetes Mellitus, Insulin-Dependent, 20
|
Digeorge Syndrome
|
Digestive System Neoplasms
|
Dihydropyrimidine Dehydrogenase Deficiency
|
Disease Susceptibility
|
Disorders Of Sex Development
|
Disruptive, Impulse Control, And Conduct Disorders
|
Distal Myopathies
|
Dog Diseases
|
Dosage-Sensitive Sex Reversal
|
Drug Eruptions
|
Dry Eye Syndromes
|
Ductus Arteriosus, Patent
|
Dwarfism
|
Dyskeratosis Congenita
|
Dyskeratosis Congenita, Autosomal Dominant
|
Dyskinesias
|
Dystonia, Dopa-Responsive
|
Dystonia, Dopa-Responsive, Due To Sepiapterin Reductase Deficiency
|
Ectodermal Dysplasia, Anhidrotic, With Immunodeficiency, Osteopetrosis, And Lymphedema
|
Ectodermal Dysplasia, Hypohidrotic, With Immune Deficiency
|
Ehlers-Danlos Syndrome
|
Ehlers-Danlos Syndrome Type 6
|
Elliptocytosis, Hereditary
|
Enchondromatosis
|
Endomyocardial Fibrosis
|
Endotoxemia
|
End Stage Liver Disease
|
Enterocolitis
|
Ependymoma
|
Epilepsy, Absence
|
Epilepsy, Generalized
|
Erythrocyte Lactate Transporter Defect
|
Exudative Vitreoretinopathy 1
|
Fabry Disease
|
Facies
|
Familial Medullary Thyroid Carcinoma
|
Fanconi Syndrome
|
Fatigue
|
Fatty Liver, Alcoholic
|
Favism
|
Female Urogenital Diseases
|
Fetal Death
|
Fetal Diseases
|
Fetal Growth Retardation
|
Fibrous Dysplasia Of Bone
|
Follicular Cyst
|
Foodborne Diseases
|
Food Hypersensitivity
|
Fractures, Bone
|
Fragile X Syndrome
|
Fragile X Tremor Ataxia Syndrome
|
Frontometaphyseal Dysplasia
|
Fundus Albipunctatus
|
Gait Disorders, Neurologic
|
Galactosemias
|
Gallstones
|
Gamma Aminobutyric Acid Transaminase Deficiency
|
Gastroparesis
|
Gaucher Disease
|
Generalized Epilepsy And Paroxysmal Dyskinesia
|
Genital Neoplasms, Female
|
Gilbert Disease
|
Gingival Hyperplasia
|
Glaucoma
|
Glaucoma, Primary Open Angle
|
Gliosarcoma
|
Gliosis
|
Glomerulonephritis
|
Glomerulonephritis, Membranoproliferative
|
Glucosephosphate Dehydrogenase Deficiency
|
Glutathione Synthetase Deficiency
|
Glutathione Synthetase Deficiency Of Erythrocytes, Hemolytic Anemia Due To
|
Glycogen Storage Disease 0, Liver
|
Glycogen Storage Disease Type Vi
|
Glycogen Storage Disease Type Vii
|
Glycogen Storage Disease Xiii
|
Goiter
|
Gonadal Dysgenesis
|
Gonadal Dysgenesis Xx Type Deafness
|
Gout
|
Gout, Hprt-Related
|
Granulomatous Disease, Chronic
|
Graves Ophthalmopathy
|
Growth Mental Deficiency Syndrome Of Myhre
|
Guanidinoacetate Methyltransferase Deficiency
|
Hand Deformities, Congenital
|
Noise-Induced Hearing Loss
|
Heart Septal Defects, Atrial
|
Helicobacter Infections
|
Hemangioma
|
Hematologic Diseases
|
Hematologic Neoplasms
|
Hematoma
|
Hemorrhoids
|
Hepatic Adenomas, Familial
|
Hepatitis, Alcoholic
|
Hepatitis, Animal
|
Hepatitis B
|
Hepatitis B, Chronic
|
Hepatitis C
|
Hepatitis C, Chronic
|
Hepatomegaly
|
Hepatorenal Syndrome
|
Hereditary Autoinflammatory Diseases
|
Hereditary Sensory And Autonomic Neuropathies
|
Hereditary Spastic Paralysis, Infantile Onset Ascending
|
Hernia, Inguinal
|
Hernia, Umbilical
|
Herpesviridae Infections
|
Holocarboxylase Synthetase Deficiency
|
Homocystinuria
|
Hoyeraal Hreidarsson Syndrome
|
Hydronephrosis
|
Hydroxykynureninuria
|
Hyperammonemia
|
Hyperbilirubinemia
|
Hyperbilirubinemia, Transient Familial Neonatal
|
Hypercalcemia
|
Hypercalciuria
|
Hypereosinophilic Syndrome
|
Hyperexplexia Hereditary
|
Hyperglycinemia, Nonketotic
|
Hyperinsulinemic Hypoglycemia, Familial, 7
|
Hyperinsulinism
|
Hyperlipidemia, Combined, 2
|
Hyperlipoproteinemias
|
Hyperlipoproteinemia Type I
|
Hyperlipoproteinemia Type Iii
|
Hypermethioninemia
|
Hyperparathyroidism, Secondary
|
Hyperphagia
|
Hyperphenylalaninemia, Bh4-Deficient, B
|
Hyperprolactinemia
|
Hypertension, Early-Onset, Autosomal Dominant, With Severe Exacerbation In Pregnancy
|
Hypertension, Portal
|
Hypertension, Pregnancy-Induced
|
Hypertension, Renal
|
Hypertriglyceridemia
|
Hyperuricemia
|
Hypokinesia
|
Hypophosphatemia
|
Hypophosphatemic Rickets, Autosomal Recessive, 2
|
Hypospadias
|
Hypothyroidism
|
Hypothyroidism, Congenital, Nongoitrous, 5
|
Ichthyosis
|
Idiopathic Basal Ganglia Calcification 1
|
Idiopathic Hypogonadotropic Hypogonadism
|
Immune Dysregulation, Polyendocrinopathy, Enteropathy, X-Linked Syndrome
|
Immunodeficiency Due To Defect In Cd3-Zeta
|
Immunodeficiency Without Anhidrotic Ectodermal Dysplasia
|
Immunologic Deficiency Syndromes
|
Incontinentia Pigmenti
|
Infant, Premature, Diseases
|
Infection
|
Intervertebral Disc Degeneration
|
Intestinal Diseases
|
Intestinal Perforation
|
Intracranial Thrombosis
|
Invasive Pneumococcal Disease, Recurrent Isolated, 1
|
Invasive Pneumococcal Disease, Recurrent Isolated, 2
|
Iridogoniodysgenesis, Dominant Type
|
Ischemic Attack, Transient
|
Jervell-Lange Nielsen Syndrome
|
Juvenile Polyposis With Hereditary Hemorrhagic Telangiectasia
|
Kallmann Syndrome
|
Keratosis
|
Kernicterus
|
Kidney Diseases, Cystic
|
Klippel-Feil Syndrome
|
Klippel Feil Syndrome Dominant Type
|
Korsakoff Syndrome
|
Lacrimoauriculodentodigital Syndrome
|
Language Disorders
|
Laron Syndrome
|
Laryngeal Neoplasms
|
Leiomyosarcoma
|
Leishmaniasis
|
Leprosy
|
Lesch-Nyhan Syndrome
|
Lethal Congenital Contracture Syndrome 2
|
Leukemia, Megakaryoblastic, Acute
|
Leukemia, Monocytic, Acute
|
Leukemia, Myelomonocytic, Acute
|
Leukemia, Myelomonocytic, Juvenile
|
Leukoencephalopathy With Brainstem And Spinal Cord Involvement And Lactate Elevation
|
Leukoplakia, Oral
|
Leydig Cell Hypoplasia
|
Leydig Cell Tumor
|
Li-Fraumeni Syndrome
|
Li-Fraumeni Syndrome 2
|
Lipoprotein Glomerulopathy
|
Liposarcoma
|
Lissencephaly
|
Liver Failure
|
Liver Failure, Acute
|
Long Qt Syndrome 2
|
Long Qt Syndrome 6
|
Lung Diseases, Obstructive
|
Lymphoma
|
Lymphoma, B-Cell
|
Lymphoma, T-Cell, Peripheral
|
Lymphopenia
|
Colorectal Cancer, Hereditary Nonpolyposis, Type 1
|
Macrophage Activation Syndrome
|
Macrothrombocytopenia Progressive Deafness
|
Macular Degeneration, Age-Related, 1
|
Macular Degeneration, Age-Related, 3
|
Macular Edema
|
Major Affective Disorder 1
|
Major Affective Disorder 7
|
Malnutrition
|
Malpuech Facial Clefting Syndrome
|
Mason-Type Diabetes
|
Maturity-Onset Diabetes Of The Young, Type 1
|
Maturity-Onset Diabetes Of The Young, Type 3
|
Meier-Gorlin Syndrome
|
Melas Syndrome
|
Meningioma
|
Meningitis
|
Meningitis, Meningococcal
|
Meningococcal Infection
|
Meningomyelocele
|
Mental Retardation, Autosomal Recessive 6
|
Mental Retardation, X-Linked 30
|
Mercury Poisoning
|
Mercury Poisoning, Nervous System
|
Metabolic Diseases
|
Metaplasia
|
Methylmalonic Acidemia With Homocystinuria
|
Microcephaly
|
Microphthalmia, Isolated 4
|
Microphthalmia, Syndromic 6
|
Microphthalmos
|
Mitochondrial Diseases
|
Mitochondrial Encephalomyopathies
|
Molybdenum Cofactor Deficiency
|
Mood Disorder
|
Mosaic Variegated Aneuploidy Syndrome
|
Motor Neuron Disease
|
Mucolipidosis Iii Gamma
|
Muir-Torre Syndrome
|
Mulibrey Nanism
|
Multiple Sclerosis, Relapsing-Remitting
|
Multiple Sulfatase Deficiency Disease
|
Muscle Hypotonia
|
Muscle Rigidity
|
Muscular Dystrophies
|
Muscular Dystrophy, Emery-Dreifuss
|
Musculoskeletal Pain
|
Mycobacterium Infections
|
Mycoplasma Infections
|
Myelodysplastic Syndromes
|
Myh9-Related Disorders
|
Myocardial Stunning
|
Myocarditis
|
Myoclonic Dystonia
|
Myoclonic Epilepsies, Progressive
|
Myopathy, Mitochondrial Progressive, With Congenital Cataract, Hearing Loss, And Developmental Delay
|
Myopathy, Myosin Storage
|
Myopathy With Lactic Acidosis And Sideroblastic Anemia
|
Myopia
|