Liver Cirrhosis, Experimental
|
Breast Carcinoma
|
Colorectal Cancer
|
Prostatic Neoplasms
|
Stomach Neoplasms
|
Mammary Neoplasms, Experimental
|
Myocardial Ischemia
|
Hepatocellular Carcinoma
|
Carcinoma
|
Disease Progression
|
Lung Neoplasms
|
Melanoma
|
Neoplasm Metastasis
|
Mammary Neoplasms, Animal
|
Polycystic Ovary Syndrome
|
Hiv Infections
|
Ovarian Neoplasms
|
Squamous Cell Carcinoma
|
Hypertension
|
Schizophrenia
|
Rheumatoid Arthritis
|
Colonic Neoplasm
|
Renal Cell Carcinoma
|
Carcinoma, Non-Small-Cell Lung
|
Heart Failure
|
Leukemia, Myeloid, Acute
|
Glioma
|
Adenocarcinoma
|
Autism
|
Carcinoma, Adenoid Cystic
|
Neoplasm Invasiveness
|
Obesity
|
Drug Dependence
|
Craniofacial Abnormalities
|
Diabetes Mellitus, Experimental
|
Urinary Bladder Neoplasms
|
Liver Neoplasms
|
Neuroblastoma
|
Disease Models, Animal
|
Diabetes Mellitus, Type 2
|
Precancerous Conditions
|
Myocardial Infarction
|
Arthritis, Juvenile
|
Mesothelioma, Malignant
|
Drug-Induced Liver Injury
|
Intellectual Disability
|
Status Epilepticus
|
Cardiomyopathies
|
Hyperalgesia
|
Endometriosis
|
Lung Adenocarcinoma
|
Cocaine Dependence
|
Peripheral Neuropathy
|
Cardiac Hypertrophy
|
Skin Neoplasms
|
Recurrence
|
Osteoarthritis
|
Dilated Cardiomyopathy
|
Cell Transformation, Neoplastic
|
Liver Neoplasms, Experimental
|
Microcephaly
|
Influenza, Human
|
Esophageal Neoplasms
|
Amphetamine-Related Disorders
|
Small Cell Lung Carcinoma
|
Epilepsy
|
Mouth Neoplasms
|
Parkinson's Disease
|
Weight Gain
|
Endometrial Neoplasm
|
Lymphoma, Large B-Cell, Diffuse
|
Neoplasms, Experimental
|
Alzheimer's Disease
|
Kidney Disease
|
Anoxia
|
Seizures
|
Drug-Related Side Effects And Adverse Reactions
|
Inflammation
|
Acute Coronary Syndrome
|
Malformations Of Cortical Development
|
Astrocytoma
|
Noonan Syndrome
|
Diabetic Nephropathy
|
Kidney Neoplasms
|
Fibrosis
|
Osteoporosis
|
Mesothelioma
|
Substance Withdrawal Syndrome
|
Head And Neck Neoplasms
|
Liver Diseases
|
Carcinoma, Squamous Cell Of Head And Neck
|
Leukemia, Myelomonocytic, Juvenile
|
Cholestasis
|
Cholangiocarcinoma
|
Neoplasm Recurrence, Local
|
Nervous System Diseases
|
Pancreatic Carcinoma
|
Nerve Degeneration
|
Acute Lymphoblastic Leukemia
|
Neoplasms
|
Nasopharyngeal Carcinoma
|
Bipolar Disorder
|
Reperfusion Injury
|
Carcinoma, Transitional Cell
|
Chronic Myelogenous Leukemia
|
Salivary Gland Neoplasm
|
Glioblastoma Multiforme
|
Skin Diseases
|
Liver Cirrhosis
|
Lung Diseases
|
Coronary Artery Disease
|
Cleft Lip
|
Osteosarcoma
|
Ulcerative Colitis
|
Left Ventricular Hypertrophy
|
Insulin Resistance
|
Heart Diseases
|
Mental Retardation, X-Linked
|
Microsatellite Instability
|
Basal Cell Carcinoma
|
Growth Disorders
|
Costello Syndrome
|
Hemangiosarcoma
|
Cardiofaciocutaneous Syndrome
|
Adrenocortical Carcinoma
|
Arsenic Poisoning
|
Parkinsonian Disorders
|
Arthritis, Experimental
|
Limb Dystonia
|
Adenoma
|
Psoriasis
|
Endotoxemia
|
Leukemia
|
Leukemia-Lymphoma, Adult T-Cell
|
Esophageal Squamous Cell Carcinoma
|
Leukemia, Promyelocytic, Acute
|
Sezary Syndrome
|
Skin Abnormalities
|
Primary Biliary Cirrhosis
|
Trigeminal Neuralgia
|
Gallbladder Neoplasm
|
Ventricular Dysfunction, Left
|
Abnormalities, Multiple
|
Medulloblastoma
|
Cone-Rod Dystrophy 2
|
Thyroid Carcinoma
|
Hepatitis, Chronic
|
Kidney Failure, Chronic
|
Necrosis
|
Acute Kidney Injury
|
Ataxia
|
Chloracne
|
Proteinuria
|
Cardiomyopathy, Familial Hypertrophic, 1
|
Cardiomyopathy, Hypertrophic
|
Hernias, Diaphragmatic, Congenital
|
Asthma
|
Prenatal Injuries
|
Thrombosis
|
Carcinogenesis
|
Hyperplasia
|
Lymphoma, T-Cell, Cutaneous
|
Diabetes Mellitus
|
Pulmonary Hypertension
|
Lymphoma, Non-Hodgkin
|
Bone Diseases, Developmental
|
Lymphoma, Mantle-Cell
|
Focal Segmental Glomerulosclerosis
|
Burkitt Lymphoma
|
Spinocerebellar Ataxia 17
|
Multiple Myeloma
|
Multiple Sclerosis
|
Ceroid Lipofuscinosis, Neuronal 1, Infantile
|
Ceroid Lipofuscinosis, Neuronal, 6
|
Glucose Intolerance
|
Dermatitis, Allergic Contact
|
Fanconi Anemia
|
Dermatitis, Contact
|
Methylmalonic Acidemia
|
Unipolar Depression
|
Lewy Body Dementia
|
Eye Abnormalities
|
Myelodysplastic Syndromes
|
Chronic Lymphocytic Leukemia
|
Uremia
|
Muscular Diseases
|
Diabetic Angiopathies
|
Hyperglycemia
|
Neurotoxicity Syndromes
|
Papilloma
|
Penile Neoplasms
|
Cataract
|
Amino Acid Metabolism, Inborn Errors
|
Idiopathic Pulmonary Fibrosis
|
Abortion, Spontaneous
|
Amyotrophic Lateral Sclerosis
|
Male Infertility
|
Hyperammonemia
|
Polycystic Kidney, Autosomal Recessive
|
Neuroendocrine Tumors
|
Drug Hypersensitivity
|
Zellweger Syndrome
|
Ischemia
|
Colorectal Neoplasms, Hereditary Nonpolyposis
|
Pseudohypoaldosteronism
|
Gastrointestinal Diseases
|
Rectum Cancer
|
Respiratory Distress Syndrome, Adult
|
Crohn's Disease
|
Epilepsy, Temporal Lobe
|
Cholestasis, Progressive Familial Intrahepatic 1
|
Brain Ischemia
|
Brain Neoplasms
|
Iga Glomerulonephritis
|
Leukemia, Myeloid
|
Myocardial Reperfusion Injury
|
Myeloproliferative Disorder
|
Atherosclerosis
|
Meier-Gorlin Syndrome
|
Heart Defects, Congenital
|
Spinal Dysraphism
|
Spinocerebellar Ataxias
|
Anemia, Hemolytic
|
Bardet-Biedl Syndrome
|
Toxic Epidermal Necrolysis
|
Molybdenum Cofactor Deficiency
|
Systemic Lupus Erythematosus
|
Adrenal Gland Neoplasms
|
Copper-Overload Cirrhosis
|
Fetal Growth Retardation
|
Lymphoma
|
Lymphoma, Follicular
|
Testicular Germ Cell Tumor
|
Lymphoma, T-Cell
|
Lymphoma, T-Cell, Peripheral
|
Pain
|
Autism Spectrum Disorder
|
Metabolism, Inborn Errors
|
Urologic Neoplasms
|
Autoimmune Disease
|
Uterine Cervical Neoplasms
|
Calcinosis
|
Hyperkinesis
|
Allergy
|
Osteochondrodysplasias
|
Leber Congenital Amaurosis
|
Acute Lung Injury
|
Leopard Syndrome
|
Tongue Neoplasms
|
Epileptic Encephalopathy, Early Infantile, 1
|
Huntington Disease
|
Age-Related Macular Degeneration
|
Tremor
|
Thoracic Aortic Aneurysm
|
De Lange Syndrome
|
Brain Stem Neoplasms
|
Myocarditis
|
Poisoning
|
Turcot Syndrome
|
Gastrointestinal Stromal Tumors
|
Creutzfeldt Jacob Disease
|
Bone Diseases
|
Diarrhea
|
Diabetic Neuropathies
|
Hemangioma, Capillary Infantile
|
Sarcoma
|
Pneumonia, Pneumococcal
|
Megalanecephaly Polymicrogyria-Polydactyly Hydrocephalus Syndrome
|
Chondrosarcoma, Mesenchymal
|
Leukoencephalopathies
|
Heart Valve Diseases
|
Systemic Scleroderma
|
Pneumonia
|
Carcinoma, Small Cell
|
Seminoma
|
Inflammatory Bowel Disease
|
Sepsis
|
Chromosomal Instability
|
Severe Combined Immunodeficiency
|
Genetic Predisposition To Disease
|
Short Rib-Polydactyly Syndrome
|
Breast Neoplasms, Male
|
Chromosome Aberrations
|
Limb Deformities, Congenital
|
Lipid Metabolism, Inborn Errors
|
Sinusitis
|
Sitosterolemia
|
Familial Medullary Thyroid Carcinoma
|
Androgenetic Alopecia
|
Nevus, Sebaceous Of Jadassohn
|
Infertility, Female
|
Hyperinsulinism
|
Muscular Atrophy
|
Infarction, Middle Cerebral Artery
|
Anaphylaxis
|
Anemia
|
Fatty Liver
|
Gallstones
|
Gliosis
|
Coloboma
|
Pheochromocytoma
|
Coxsackievirus Infections
|
Female Urogenital Diseases
|
Distal Myopathies
|
Liver Diseases, Parasitic
|
Liver Failure, Acute
|
Hamartoma Syndrome, Multiple
|
Non-Alcoholic Fatty Liver Disease
|
Mucocutaneous Lymph Node Syndrome
|
Furlong Syndrome
|
Adenomatous Polyposis Coli
|
Mouth Diseases
|
Developmental Disabilities
|
Stargardt Disease 1
|
Hypertrophy
|
Uveal Melanoma
|
Coronary Stenosis
|
Paranoid Disorders
|
Colonic Polyps
|
Paralysis
|
Occupational Diseases
|
Hyperlipidemias
|
Pfeiffer Type Acrocephalosyndactyly
|
Amnesia
|
Congenital Hyperinsulinism
|
Marijuana Dependence
|
Micronuclei, Chromosome-Defective
|
Lymphoma, Large-Cell, Anaplastic
|
Idiopathic Hypogonadotropic Hypogonadism
|
Peroxisome Biogenesis Disorders
|
Optic Atrophy
|
Diabetes Mellitus, Permanent Neonatal
|
Hypercholesterolemia
|
Thoracic Diseases
|
Pancreatitis
|
Diabetes Mellitus, Type 1
|
Hypoxia-Ischemia, Brain
|
Neovascularization, Pathologic
|
Atrophy
|
Dyslipidemias
|
Thromboembolism
|
Intracerebral Hemorrhage
|
Jackson-Weiss Syndrome
|
Precursor T-Cell Lymphoblastic Leukemia-Lymphoma
|
Propionic Acidemia
|
Alternating Hemiplegia Of Childhood
|
Prostatic Intraepithelial Neoplasia
|
Amyotrophic Lateral Sclerosis 1
|
Porokeratosis, Disseminated Superficial Actinic 1
|
Brain Diseases
|
Thyroid Cancer, Follicular
|
Dystonic Disorders
|
Intestinal Neoplasms
|
Embryo Loss
|
Kallmann Syndrome
|
Coffin-Siris Syndrome
|
Psychomotor Disorders
|
Psychoses, Substance-Induced
|
Aneurysm, Dissecting
|
Dwarfism
|
Chronic Obstructive Pulmonary Disease
|
Nervous System Malformations
|
Deafness
|
Cardiomyopathy, Hypertrophic, Familial
|
Pulmonary Veno-Occlusive Disease
|
Bare Lymphocyte Syndrome, Type I
|
Cardiovascular Disease
|
Aneuploidy
|
Alcohol Dependence
|
Radiation Injuries, Experimental
|
Lacrimoauriculodentodigital Syndrome
|
Brain Injuries
|
Thyroid Cancer, Papillary
|
Hepatolenticular Degeneration
|
Neural Tube Defects
|
Enterocolitis, Necrotizing
|
Hepatic Encephalopathy
|
Cholestasis, Intrahepatic
|
Memory Disorders
|
Ependymoma
|
Epidermal Nevus
|
Lymphoproliferative Syndrome, Ebv-Associated, Autosomal, 1
|
Colorectal Cancer, Hereditary Nonpolyposis, Type 1
|
Macrophage Activation Syndrome
|
Macrothrombocytopenia, Autosomal Dominant, Tubb1-Related
|
Macrothrombocytopenia Progressive Deafness
|
Macular Degeneration, Age-Related, 2
|
Male Infertility With Large-Headed, Multiflagellar, Polyploid Spermatozoa
|
Malonic Aciduria
|
Mandibular Neoplasms
|
Manganese Poisoning
|
Marfan Syndrome
|
Mason-Type Diabetes
|
Massive Hepatic Necrosis
|
Mastocytosis, Systemic
|
Maturity-Onset Diabetes Of The Young, Type 2
|
Mckusick Kaufman Syndrome
|
Megacystis Microcolon Intestinal Hypoperistalsis Syndrome
|
Megalencephaly
|
Melorheostosis
|
Meningioma
|
Menkes Kinky Hair Syndrome
|
Mental Retardation And Microcephaly With Pontine And Cerebellar Hypoplasia
|
Mental Retardation-Hypotonic Facies Syndrome, X-Linked, 1
|
Mental Retardation, X-Linked 30
|
Mental Retardation, X-Linked 63
|
Mental Retardation, X-Linked 72
|
Mental Retardation, X-Linked, Syndromic 14
|
Mesenteric Vascular Occlusion
|
Metatropic Dwarfism
|
Methylmalonic Aciduria Cbla Type
|
Methylmalonic Aciduria Cblb Type
|
Mevalonate Kinase Deficiency
|
Microvillus Inclusion Disease
|
Migraine Disorder
|
Mitochondrial Complex I Deficiency
|
Mitochondrial Complex Iii Deficiency
|
Mitochondrial Diseases
|
Mitochondrial Encephalomyopathies
|
Mitochondrial Myopathies
|
Mood Disorder
|
Mosaic Variegated Aneuploidy Syndrome
|
Motor Skills Disorders
|
Muenke Syndrome
|
Muir-Torre Syndrome
|
Multiple Endocrine Neoplasia
|
Multiple Endocrine Neoplasia Type 2a
|
Multiple Endocrine Neoplasia Type 2b
|
Muscle Rigidity
|
Muscular Atrophy, Spinal
|
Muscular Dystrophy, Animal
|
Muscular Dystrophy, Facioscapulohumeral
|
Muscular Dystrophy, Oculopharyngeal
|
Musculoskeletal Pain
|
Myasthenia Gravis
|
Myasthenic Syndrome, Congenital, Type Id
|
Myeloproliferative Disorder, Chronic, With Eosinophilia
|
Myh9-Related Disorders
|
Myocardial Stunning
|
Myoclonic Epilepsies, Progressive
|
Myopathies, Structural, Congenital
|
Myopathy, Myosin Storage
|
Myopathy With Lactic Acidosis And Sideroblastic Anemia
|
Myositis
|
Myositis, Inclusion Body
|
Myositis Ossificans
|
Myotonia
|
Myotonic Dystrophy
|
Narcolepsy
|
Nasopharyngeal Neoplasm
|
Nemaline Myopathy 3
|
Neointima
|
Neoplasms, Glandular And Epithelial
|
Neoplasms, Second Primary
|
Neoplasms, Squamous Cell
|
Neoplastic Processes
|
Alport Syndrome, X-Linked
|
Nephrogenic Fibrosing Dermopathy
|
Nephrolithiasis, X-Linked Recessive, With Renal Failure
|
Neuropathic Pain
|
Neuralgia, Postherpetic
|
Neural Tube Defect, Folate-Sensitive
|
Neurilemmoma
|
Neurodegenerative Diseases
|
Neuroectodermal Tumors, Primitive
|
Neuroectodermal Tumors, Primitive, Peripheral
|
Neurofibroma, Plexiform
|
Neurofibromatosis 1
|
Neurofibrosarcoma
|
Neurogenic Inflammation
|
Neurologic Manifestations
|
Neuronal Ceroid-Lipofuscinoses
|
Neuronopathy, Distal Hereditary Motor, Type V
|
Neuropathy, Hereditary Sensory, With Spastic Paraplegia, Autosomal Recessive
|
Neutropenia
|
Neutrophil Immunodeficiency Syndrome
|
Nicolaides Baraitser Syndrome
|
Night Blindness, Congenital Stationary, Autosomal Dominant 3
|
Nijmegen Breakage Syndrome-Like Disorder
|
Noonan Syndrome 3
|
Noonan Syndrome 5
|
Noonan Syndrome 6
|
Occipital Horn Syndrome
|
Oguchi Disease
|
Oligospermia
|
Opitz-Kaveggia Syndrome
|
Optic Atrophy 1 And Deafness
|
Optic Atrophy, Autosomal Dominant
|
Optic Atrophy Polyneuropathy Deafness
|
Osler-Rendu-Weber Syndrome 2
|
Osseous Heteroplasia, Progressive
|
Ossification, Heterotopic
|
Osteoglophonic Dwarfism
|
Osteopetrosis
|
Osteopetrosis, Autosomal Recessive 4
|
Ovarian Cysts
|
Ovarian Epithelial Cancer
|
Pancreatitis, Chronic
|
Paraplegia
|
Parastremmatic Dwarfism
|
Parkinson Disease 6, Autosomal Recessive Early-Onset
|
Parkinson Disease, Secondary
|
Pemphigus, Benign Familial
|
Penile Diseases
|
Peritoneal Neoplasms
|
Peritonitis
|
Persistent Fetal Circulation Syndrome
|
Persistent Müllerian Duct Syndrome
|
Peutz-Jeghers Syndrome
|
Phencyclidine Abuse
|
Phosphoenolpyruvate Carboxykinase 2 Deficiency
|
Phosphoenolpyruvate Carboxykinase Deficiency
|
Phosphoglycerate Kinase 1 Deficiency
|
Phosphoribosylpyrophosphate Synthetase Superactivity
|
Piebaldism
|
Pigmented Nodular Adrenocortical Disease, Primary, 1
|
Plagiocephaly, Nonsynostotic
|
Plasma Cell Granuloma, Pulmonary
|
Pleuropulmonary Blastoma
|
Pneumoconiosis
|
Polycythemia
|
Polycythemia Vera
|
Polydactyly
|
Polymicrogyria With Optic Nerve Hypoplasia
|
Polyploidy
|
Polyposis Syndrome, Hereditary Mixed, 2
|
Polyuria
|
Pontocerebellar Hypoplasia Type 1
|
Pontocerebellar Hypoplasia Type 6
|
Port-Wine Stain
|
Preeclampsia
|
Pregnancy Complications
|
Prenatal Exposure Delayed Effects
|
Primary Ciliary Dyskinesia, 3
|
Primary Myelofibrosis
|
Progressive External Ophthalmoplegia With Mitochondrial Dna Deletions, Autosomal Dominant, 3
|
Progressive Familial Heart Block, Type Ib
|
Prostate Cancer, Familial
|
Pruritus
|
Pseudohypoparathyroidism
|
Pseudohypoparathyroidism Type 1b
|
Pseudopseudohypoparathyroidism
|
Pseudoxanthoma Elasticum
|
Psychosis
|
Puberty, Precocious
|
Pulmonary Edema Of Mountaineers
|
Pulmonary Embolism
|
Pulmonary Fibrosis
|
Purine-Pyrimidine Metabolism, Inborn Errors
|
Pyelonephritis
|
Pyruvate Dehydrogenase E2 Deficiency
|
Pyruvate Kinase Deficiency Of Red Cells
|
Raine Syndrome
|
Rapadilino Syndrome
|
Refractive Errors
|
Renal Insufficiency
|
Respiration Disorders
|
Respiratory Hypersensitivity
|
Respiratory Insufficiency
|
Respiratory System Abnormalities
|
Respiratory Tract Diseases
|
Reticular Dysgenesis
|
Retinal Degeneration
|
Retinal Detachment
|
Retinitis Pigmentosa 10
|
3-Methylcrotonyl Coa Carboxylase 1 Deficiency
|
Retinitis Pigmentosa 2
|
Retinitis Pigmentosa 33
|
Rett Syndrome
|
Rhabdoid Tumor Predisposition Syndrome 2
|
Rhabdomyosarcoma, Embryonal
|
Rhinitis
|
Rickettsia Infections
|
Robinow Syndrome, Autosomal Recessive
|
Rothmund-Thomson Syndrome
|
Sarcoidosis
|
Sarcoidosis, Early-Onset
|
Ewing Sarcoma
|
Sarcopenia
|
Scaphocephaly, Maxillary Retrusion, And Mental Retardation
|
Schimke Immunoosseous Dysplasia
|
Seckel Syndrome 1
|
Sensory Ataxic Neuropathy, Dysarthria, And Ophthalmoparesis
|
Sesame Syndrome
|
Short Rib-Polydactyly Syndrome, Verma-Naumoff Type
|
N-Acetylneuraminic Acid Storage Disease
|
Sick Sinus Syndrome
|
Sick Sinus Syndrome 2, Autosomal Dominant
|
Situs Inversus
|
Sjogren Syndrome
|
Spastic Paraplegia 13, Autosomal Dominant
|
Spastic Paraplegia 3, Autosomal Dominant
|
Spastic Paraplegia 4, Autosomal Dominant
|
Spastic Paraplegia 7, Autosomal Recessive
|
Spermatogenic Failure, Nonobstructive, Y-Linked
|
Spherocytosis, Hereditary
|
Spinal Muscular Atrophy, Distal, X-Linked 3
|
Spinal Muscular Atrophy With Respiratory Distress 1
|
Spinocerebellar Ataxia 14
|
Spinocerebellar Ataxia 28
|
Spinocerebellar Ataxia, Autosomal Recessive 1
|
Spinocerebellar Ataxia, Autosomal Recessive 9
|
Splenic Neoplasms
|
Splenomegaly
|
Spondylodysplasia And Premature Pubarche
|
Spondylometaepiphyseal Dysplasia, Short Limb-Hand Type
|
Spondylometaphyseal Dysplasia, Kozlowski Type
|
Stroke
|
Sturge-Weber Syndrome
|
Sunburn
|
Progressive Supranuclear Palsy
|
Surfactant Metabolism Dysfunction, Pulmonary, 3
|
Systemic Carnitine Deficiency
|
Tachycardia
|
Tangier Disease
|
Tarp Syndrome
|
T Cell Immunodeficiency Primary
|
Telangiectasia, Hereditary Hemorrhagic
|
Thanatophoric Dysplasia, Type 2
|
Thanatophoric Dysplasia
|
Thoracic Neoplasms
|
Thrombocythemia, Essential
|
Thrombocytopenia
|
Thrombocytosis
|
Thyroid Cancer, Medullary
|
Tick-Borne Diseases
|
Tooth Abnormalities
|
Tyrosine Kinase 2 Deficiency
|
Uridine 5-Prime Monophosphate Hydrolase Deficiency, Hemolytic Anemia Due To
|
Urination Disorders
|
Usher Syndromes
|
Usher Syndrome, Type 1b
|
Uterine Neoplasms
|
Uveitis
|
Vascular Diseases
|
Vascular Malformations
|
Vascular System Injuries
|
Venous Malformations, Multiple Cutaneous And Mucosal
|
Venous Thrombosis
|
Vestibular Diseases
|
Visceral Myopathy, Familial
|
Vitamin A Deficiency
|
Vitamin B 12 Deficiency
|
Werner Syndrome
|
Williams Syndrome
|
Wolcott-Rallison Syndrome
|
Wolff-Parkinson-White Syndrome
|
Xanthomatosis
|
Xeroderma Pigmentosum, Complementation Group B
|
Xeroderma Pigmentosum, Complementation Group D
|
Retinitis Pigmentosa 19
|
3-Methylcrotonyl Coa Carboxylase 2 Deficiency
|
Abnormalities, Drug-Induced
|
Abruptio Placentae
|
Absent Radii And Thrombocytopenia
|
Achondroplasia
|
Achromatopsia 2
|
Achromatopsia 3
|
Acidosis, Lactic
|
Acrocallosal Syndrome
|
Acrocephalopolysyndactyly Type Ii
|
Acrocephalosyndactylia
|
Acromegaly
|
Acromesomelic Dysplasia, Maroteaux Type
|
Acth-Secreting Pituitary Adenoma
|
Addison Disease
|
Adenocarcinoma, Follicular
|
Adenocarcinoma Of Esophagus
|
Adenoma, Liver Cell
|
Adenosine Triphosphate, Elevated, Of Erythrocytes
|
Adenylate Kinase Deficiency, Hemolytic Anemia Due To
|
Adrenal Hyperplasia, Congenital
|
Adrenoleukodystrophy
|
Afibrinogenemia
|
Agammaglobulinemia
|
Aging, Premature
|
Aicardi-Goutieres Syndrome
|
Albright's Hereditary Osteodystrophy
|
Albuminuria
|
Alcohol-Induced Disorders, Nervous System
|
Alopecia, Neurologic Defects, And Endocrinopathy Syndrome
|
Alpha-Thalassemia Myelodysplasia Syndrome
|
Alveolar Capillary Dysplasia
|
Ameloblastoma
|
Amyloidosis, Familial
|
Amyotrophic Lateral Sclerosis 10
|
Amyotrophic Lateral Sclerosis 4, Juvenile
|
Amyotrophic Lateral Sclerosis 6, Autosomal Recessive
|
Anemia, Diamond-Blackfan, 3
|
Anemia, Hemolytic, Congenital Nonspherocytic
|
Anemia, Hypoplastic, Congenital
|
Sickle Cell Anemia
|
Anemia, Sideroblastic
|
Anemia, Sideroblastic Spinocerebellar Ataxia
|
Angelman Syndrome
|
Ankylosis
|
Antley-Bixler Syndrome Phenotype
|
Aortic Aneurysm
|
Aortic Aneurysm, Familial Thoracic 4
|
Aortic Aneurysm, Familial Thoracic 6
|
Aortic Rupture
|
Apparent Mineralocorticoid Excess
|
Arthralgia
|
Psoriatic Arthritis
|
Arthrogryposis Multiplex Congenita, Distal, X-Linked
|
Arts Syndrome
|
Asbestosis
|
Ataxia Telangiectasia
|
Atrial Fibrillation
|
Atrial Myxoma, Familial
|
Atrial Septal Defect 5
|
Atrioventricular Block
|
Atr-X Syndrome
|
Atypical Hemolytic Uremic Syndrome
|
Auditory Neuropathy, Autosomal Dominant, 1
|
Autoimmune Lymphoproliferative Syndrome
|
Azoospermia
|
Bare Lymphocyte Syndrome 2
|
Bartter Syndrome
|
Bartter Syndrome, Antenatal , Type 2
|
Basal Ganglia Diseases
|
Beta-Thalassemia
|
Bile Duct Neoplasms
|
Biliary Tract Neoplasms
|
Birth Weight
|
Bjornstad Syndrome
|
Blast Crisis
|
Blau Syndrome
|
Blood Coagulation Disorders
|
Bloom Syndrome
|
Body Weight
|
Bone Marrow Diseases
|
Bone Neoplasms
|
Bowen's Disease
|
Brachial Plexus Neuritis
|
Brachydactyly
|
Brachydactyly Type A2
|
Brachydactyly, Type B1
|
Brachyolmia Type 3
|
Bradycardia
|
Brain Diseases, Metabolic, Inborn
|
Brain Edema
|
Brody Myopathy
|
Bronchiectasis With Or Without Elevated Sweat Chloride 1
|
Brugada Syndrome 8
|
Bruton Type Agammaglobulinemia
|
Budd-Chiari Syndrome
|
Burns, Chemical
|
Buschke-Ollendorff Syndrome
|
Cafe-Au-Lait Spots
|
Cafe Au Lait Spots, Multiple
|
Calcification Of Joints And Arteries
|
Cantu Syndrome
|
Carbamoyl-Phosphate Synthase I Deficiency Disease
|
Carbohydrate Metabolism, Inborn Errors
|
Carcinoma, Medullary
|
Carcinoma, Pancreatic Ductal
|
Cardiomyopathy, Dilated, 1dd
|
Cardiomyopathy, Dilated, 1ee
|
Cardiomyopathy, Dilated, 1o
|
Cardiomyopathy, Dilated, 1s
|
Cardiomyopathy, Familial Hypertrophic, 11
|
Cardiomyopathy, Familial Hypertrophic, 14
|
Cardiomyopathy, Familial Hypertrophic, 6
|
Carney Complex
|
Carney Complex Variant
|
Carotid Artery Diseases
|
Catalepsy
|
Cataract And Cardiomyopathy
|
Catshl Syndrome
|
Cecal Neoplasms
|
Celiac Disease
|
Cerebellar Ataxia
|
Cerebellar Diseases
|
Cerebral Infarction
|
Cerebrooculofacioskeletal Syndrome 2
|
Charcot-Marie-Tooth Disease
|
Charcot-Marie-Tooth Disease, Axonal, Type 2a1
|
Charcot-Marie-Tooth Disease, Axonal, Type 2a2
|
Charcot-Marie-Tooth Disease, Axonal, Type 2n
|
Charcot-Marie-Tooth Disease, Dominant Intermediate B
|
Charcot-Marie-Tooth Disease, Dominant Intermediate C
|
Charcot-Marie-Tooth Disease, Type 2d
|
Charge Syndrome
|
Chilblain Lupus 1
|
Cholangitis
|
Sclerosing Cholangitis
|
Choledochal Cyst
|
Cholestasis, Benign Recurrent Intrahepatic, 2
|
Cholestasis, Progressive Familial Intrahepatic 3
|
Chondrodysplasia, Acromesomelic, With Genital Anomalies
|
Chondrosarcoma, Extraskeletal Myxoid
|
Chromosome 2q37 Deletion Syndrome
|
Chromosome Breakage
|
Chromosome Xp11.3 Deletion Syndrome
|
Chudley-Mccullough Syndrome
|
Chylomicron Retention Disease
|
Citrullinemia
|
Clear-Cell Metastatic Renal Cell Carcinoma
|
Coffin-Lowry Syndrome
|
Cognitive Impairment
|
Colitis
|
Color Vision Defects
|
Coma
|
Combined Oxidative Phosphorylation Deficiency 1
|
Combined Oxidative Phosphorylation Deficiency 4
|
Cone Dystrophy 4
|
Cone-Rod Dystrophy 3
|
Congenital Abnormalities
|
Congenital Bilateral Aplasia Of Vas Deferens
|
Congenital Central Hypoventilation Syndrome
|
Conjunctival Diseases
|
Corneal Dystrophy, Fleck
|
Coronary Aneurysm
|
Coronary Heart Disease
|
Coronary Vessel Anomalies
|
Craniofacial Dysostosis
|
Craniopharyngioma
|
Craniosynostoses
|
Craniosynostosis Radial Aplasia Syndrome
|
Crouzon Syndrome With Acanthosis Nigricans
|
Cryopyrin-Associated Periodic Syndromes
|
Cryptorchidism
|
Cushing Syndrome
|
Cutis Gyrata Syndrome Of Beare And Stevenson
|
Cystic Fibrosis
|
Darier Disease
|
Deafness, Aminoglycoside-Induced
|
Deafness, Autosomal Dominant 11
|
Deafness, Autosomal Dominant 20
|
Deafness, Autosomal Dominant 48
|
Deafness, Autosomal Dominant Nonsyndromic Sensorineural 17
|
Deafness, Autosomal Recessive 12
|
Deafness, Autosomal Recessive 2
|
Deafness, Autosomal Recessive 30
|
Deafness, Autosomal Recessive 37
|
Deafness, X-Linked 1
|
Demyelinating Diseases
|
Dent Disease
|
Dent Disease 1
|
Deoxyguanosine Kinase Deficiency
|
Atopic Eczema
|
Diabetes Insipidus, Nephrogenic
|
Diabetes Mellitus, Insulin-Dependent, 19
|
Diabetes Mellitus, Insulin-Resistant, With Acanthosis Nigricans
|
Diabetes Mellitus, Transient Neonatal, 2
|
Diabetic Cardiomyopathies
|
Digestive System Neoplasms
|
Dihydropyrimidine Dehydrogenase Deficiency
|
Distal Arthrogryposis Type 2b
|
Distal Myopathy, Nonaka Type
|
Dna Repair-Deficiency Disorders
|
Dog Diseases
|
Donohue Syndrome
|
Double Outlet Right Ventricle
|
Down Syndrome
|
Dyskinesia, Drug-Induced
|
Dysostoses
|
Dystonia 12
|
Dystonia 3, Torsion, X-Linked
|
Dystonia, Dopa-Responsive
|
Dystonia Musculorum Deformans Type 1
|
Edema
|
Endocrine-Cerebroosteodysplasia
|
Endocrine System Diseases
|
Endometrial Hyperplasia
|
End Stage Liver Disease
|
Enterocolitis
|
Enterovirus Infections
|
Epileptic Encephalopathy, Early Infantile, 2
|
Epileptic Encephalopathy, Lennox-Gastaut Type
|
Erythema
|
Esophageal Diseases
|
Esophagitis
|
Exanthema
|
Eye Diseases, Hereditary
|
Familial Cold Autoinflammatory Syndrome 2
|
Familial Hypophosphatemic Rickets
|
Familial Primary Pulmonary Hypertension
|
Fanconi Anemia, Complementation Group J
|
Fatigue
|
Fetal Death
|
Fetal Diseases
|
Fever
|
Fibrosis Of Extraocular Muscles, Congenital, 3a, With Or Without Extraocular Involvement
|
Fibrosis Of Extraocular Muscles, Congenital, 3b
|
Fibrous Dysplasia, Polyostotic
|
Finnish Lethal Neonatal Metabolic Syndrome
|
Food Hypersensitivity
|
Fractures, Bone
|
Freeman-Sheldon Syndrome
|
Frontotemporal Lobar Degeneration
|
Fructosuria
|
Galactosemias
|
Gallbladder Disease 4
|
Gamma-Glutamylcysteine Synthetase Deficiency, Hemolytic Anemia Due To
|
Gastrointestinal Neoplasms
|
Glaucoma
|
Glutamine Deficiency, Congenital
|
Glutathione Synthetase Deficiency
|
Glutathione Synthetase Deficiency Of Erythrocytes, Hemolytic Anemia Due To
|
Glycogen Storage Disease Ixc
|
Glycogen Storage Disease Of Heart, Lethal Congenital
|
Glycogen Storage Disease Type V
|
Glycogen Storage Disease Type Vi
|
Glycogen Storage Disease Type Vii
|
Goiter
|
Gout, Hprt-Related
|
Granuloma, Plasma Cell
|
Graves Disease
|
Griscelli Syndrome Type 1
|
Griscelli Syndrome Type 2
|
Growth Hormone-Secreting Pituitary Adenoma
|
Hair Diseases
|
Harlequin Type Ichthyosis
|
Noise-Induced Hearing Loss
|
Hearing Loss, Sensorineural
|
Heartburn
|
Heart Septal Defects, Atrial
|
Heart Septal Defects, Ventricular
|
Hecht Syndrome
|
Hematologic Neoplasms
|
Hemiplegic Migraine, Familial Type 2
|
Hemolysis
|
Hemorrhagic Disorders
|
Hepatitis
|
Hepatitis B, Chronic
|
Hepatitis C
|
Hereditary Autoinflammatory Diseases
|
Hereditary Macular Coloboma
|
Hereditary Motor And Sensory Neuropathy, Type Iic
|
Hereditary Motor And Sensory Neuropathy Vi
|
Hereditary Pancreatitis
|
Hereditary Renal Agenesis
|
Hereditary Sensory And Autonomic Neuropathies
|
Hernia, Diaphragmatic
|
Hernia, Inguinal
|
Herpesviridae Infections
|
Heterotaxy Syndrome
|
Hirschsprung Disease
|
Holocarboxylase Synthetase Deficiency
|
Hydrolethalus Syndrome
|
Hyperaldosteronism
|
Hyperandrogenism
|
Hyperbilirubinemia
|
Hypercalciuria, Absorptive, 2
|
Hypereosinophilic Syndrome
|
Hyperexplexia Hereditary
|
Hyperglycerolemia
|
Hyperinsulinemic Hypoglycemia, Familial, 3
|
Hyperinsulinemic Hypoglycemia, Familial, 5
|
Hyperinsulinemic Hypoglycemia, Familial, 6
|
Hyperkeratosis, Epidermolytic
|
Hypercholesterolemia, Familial
|
Hypermethioninemia
|
Hyperphagia
|
Hyperphenylalaninemia, Bh4-Deficient, B
|
Hypertension, Renal
|
Hyperuricemia
|
Familial Hdl Deficiency
|
Hypochondroplasia
|
Hypogammaglobulinemia And Isolated Growth Hormone Deficiency, X-Linked
|
Hypoglycemia, Leucine-Induced
|
Hypogonadism
|
Hypokinesia
|
Hypomagnesemia 1, Intestinal
|
Hyponatremia
|
Ichthyosis
|
Ichthyosis, Lamellar
|
Ichthyosis Prematurity Syndrome
|
Iga Deficiency
|
Immune System Disease
|
Immunoblastic Lymphadenopathy
|
Immunologic Deficiency Syndromes
|
Inclusion Body Myopathy Autosomal Recessive
|
Inclusion Body Myopathy With Early-Onset Paget Disease And Frontotemporal Dementia
|
Inflammatory Breast Neoplasms
|
Influenza In Birds
|
Inherited Peripheral Neuropathy
|
Insulin-Like Growth Factor I, Resistance To
|
Intestinal Diseases
|
Intestinal Polyposis
|
Intrahepatic Cholestasis Of Pregnancy
|
Invasive Pneumococcal Disease, Recurrent Isolated, 1
|
Irak4 Deficiency
|
Ischemic Attack, Transient
|
Jaundice, Chronic Idiopathic
|
Jaundice, Obstructive
|
Jaw Abnormalities
|
Joubert Syndrome 8
|
Juvenile-Onset Dystonia
|
Juvenile Polyposis Syndrome
|
Keloid
|
Keratoacanthoma Familial
|
Keratomalacia
|
Keratosis, Seborrheic
|
Kidney Stone
|
Kufor-Rakeb Syndrome
|
Lactose Intolerance, Adult Type
|
Lamellar Ichthyosis, Type 2
|
Language Development Disorders
|
Language Disorders
|
Lead Poisoning
|
Learning Disorders
|
Leigh Disease
|
Leopard Syndrome, 2
|
Leprosy
|
Lesch-Nyhan Syndrome
|
Lethal Congenital Contractural Syndrome 3
|
Lethal Congenital Contracture Syndrome 2
|
Leukemia, Erythroblastic, Acute
|
Leukemia, Hairy Cell
|
Leukemia, Megakaryoblastic, Of Down Syndrome
|
Leukemia, Myelomonocytic, Acute
|
Leukodystrophy, Hypomyelinating, 4
|
Leukoencephalopathy With Brainstem And Spinal Cord Involvement And Lactate Elevation
|
Li-Fraumeni Syndrome
|
Li-Fraumeni Syndrome 2
|
Lig4 Syndrome
|
Lipidoses
|
Lipodystrophy
|
Lipodystrophy, Familial Partial
|
Liposarcoma
|
Liposarcoma, Myxoid
|
Lissencephaly 3
|
Liver Diseases, Alcoholic
|
Low Molecular Weight Proteinuria With Hypercalciuria And Nephrocalcinosis
|
Lung Injury
|
Lymphatic Metastasis
|
Lymphedema
|
Lymphoma, B-Cell
|