Breast Carcinoma
|
Liver Cirrhosis, Experimental
|
Prostatic Neoplasms
|
Hepatocellular Carcinoma
|
Lung Neoplasms
|
Stomach Neoplasms
|
Neoplasm Metastasis
|
Hypertension
|
Colorectal Cancer
|
Colonic Neoplasm
|
Adenocarcinoma
|
Diabetes Mellitus, Type 2
|
Obesity
|
Renal Cell Carcinoma
|
Cell Transformation, Neoplastic
|
Carcinoma
|
Carcinoma, Non-Small-Cell Lung
|
Neoplasm Invasiveness
|
Mammary Neoplasms, Experimental
|
Disease Models, Animal
|
Diabetes Mellitus, Experimental
|
Craniofacial Abnormalities
|
Squamous Cell Carcinoma
|
Drug-Induced Liver Injury
|
Liver Neoplasms
|
Alzheimer's Disease
|
Mammary Neoplasms, Animal
|
Myocardial Ischemia
|
Osteoarthritis
|
Parkinson's Disease
|
Inflammation
|
Autism
|
Reperfusion Injury
|
Melanoma
|
Nerve Degeneration
|
Urinary Bladder Neoplasms
|
Myocardial Infarction
|
Atherosclerosis
|
Schizophrenia
|
Hiv Infections
|
Ovarian Neoplasms
|
Rheumatoid Arthritis
|
Brain Ischemia
|
Heart Failure
|
Mesothelioma, Malignant
|
Disease Progression
|
Esophageal Neoplasms
|
Arthritis, Juvenile
|
Intellectual Disability
|
Liver Cirrhosis
|
Esophageal Squamous Cell Carcinoma
|
Leukemia, Myeloid, Acute
|
Cardiomyopathies
|
Glioma
|
Lung Adenocarcinoma
|
Neoplasms, Experimental
|
Acute Kidney Injury
|
Psoriasis
|
Fibrosis
|
Pulmonary Fibrosis
|
Asthma
|
Neurodegenerative Diseases
|
Precancerous Conditions
|
Skin Neoplasms
|
Pancreatic Carcinoma
|
Myocardial Reperfusion Injury
|
Polycystic Ovary Syndrome
|
Seizures
|
Amphetamine-Related Disorders
|
Weight Gain
|
Intracerebral Hemorrhage
|
Abortion, Spontaneous
|
Kidney Disease
|
Autoimmune Disease
|
Necrosis
|
Dermatitis, Contact
|
Skin Diseases
|
Hyperalgesia
|
Hypotension
|
Liver Diseases
|
Insulin Resistance
|
Cardiomyopathy, Hypertrophic
|
Crohn's Disease
|
Arthritis, Experimental
|
Status Epilepticus
|
Neoplasms
|
Amyotrophic Lateral Sclerosis 1
|
Acute Coronary Syndrome
|
Brain Injuries
|
Lymphoma, Large B-Cell, Diffuse
|
Diabetes Mellitus
|
Cocaine Dependence
|
Endometrial Neoplasm
|
Mesothelioma
|
Osteosarcoma
|
Kidney Failure, Chronic
|
Epilepsy
|
Male Infertility
|
Learning Disorders
|
Neoplasm Recurrence, Local
|
Fatty Liver
|
Memory Disorders
|
Lewy Body Dementia
|
Nervous System Diseases
|
Mouth Neoplasms
|
Dilated Cardiomyopathy
|
Arsenic Poisoning
|
Anoxia
|
Parkinsonian Disorders
|
Brain Neoplasms
|
Head And Neck Neoplasms
|
Peripheral Neuropathy
|
Hyperkinesis
|
Drug-Related Side Effects And Adverse Reactions
|
Cardiac Hypertrophy
|
Proteinuria
|
Cholangiocarcinoma
|
Small Cell Lung Carcinoma
|
Liver Failure, Acute
|
Lymphoma, T-Cell, Cutaneous
|
Glomerulonephritis
|
Liver Neoplasms, Experimental
|
Edema
|
Retinal Diseases
|
Osteoporosis
|
Multiple Myeloma
|
Glioblastoma Multiforme
|
Ischemia
|
Diabetic Nephropathy
|
Acute Lymphoblastic Leukemia
|
Substance Withdrawal Syndrome
|
Hemangiosarcoma
|
Pain
|
Systemic Lupus Erythematosus
|
Hyperglycemia
|
Keloid
|
Astrocytoma
|
Ulcerative Colitis
|
Anxiety Disorder
|
Hepatolenticular Degeneration
|
Calcinosis
|
Neuroblastoma
|
Carcinoma, Squamous Cell Of Head And Neck
|
Lymphoma, Non-Hodgkin
|
Heart Diseases
|
Leukemia-Lymphoma, Adult T-Cell
|
Tachycardia
|
Psychoses, Substance-Induced
|
Vascular Diseases
|
Drug Dependence
|
Stroke
|
Carcinoma, Transitional Cell
|
Carcinoma, Adenoid Cystic
|
Hyperplasia
|
Infertility, Female
|
Nasopharyngeal Carcinoma
|
Cognitive Impairment
|
Lung Diseases
|
Cardiovascular Disease
|
Amyotrophic Lateral Sclerosis
|
Coronary Artery Disease
|
Sezary Syndrome
|
Ceroid Lipofuscinosis, Neuronal 1, Infantile
|
Heart Valve Diseases
|
Endometriosis
|
Enterocolitis, Necrotizing
|
Manganese Poisoning
|
Autism Spectrum Disorder
|
Toxic Epidermal Necrolysis
|
Leukemia
|
Medulloblastoma
|
Thyroid Carcinoma
|
Uterine Cervical Neoplasms
|
Albuminuria
|
Alcoholic Liver Cirrhosis
|
Adrenocortical Carcinoma
|
Lymphoma, T-Cell
|
Non-Alcoholic Fatty Liver Disease
|
Oral Submucous Fibrosis
|
Pancreatitis
|
Genetic Predisposition To Disease
|
Allergy
|
Diabetes Mellitus, Type 1
|
Age-Related Macular Degeneration
|
Pneumonia
|
Poisoning
|
Lymphatic Metastasis
|
Diabetic Angiopathies
|
Cholestasis
|
Multiple Sclerosis
|
Radiation Injuries, Experimental
|
Dyslipidemias
|
Recurrence
|
Gallbladder Neoplasm
|
Muscular Diseases
|
Influenza, Human
|
Heart Defects, Congenital
|
Hypertrophy
|
Weight Loss
|
Fever
|
Bipolar Disorder
|
Hepatitis, Chronic
|
Diabetic Cardiomyopathies
|
Chronic Lymphocytic Leukemia
|
Trigeminal Neuralgia
|
Chronic Obstructive Pulmonary Disease
|
Uveitis
|
Stomach Ulcer
|
Hyperhomocysteinemia
|
Cataract
|
Catalepsy
|
Muscular Atrophy
|
Hypoglycemia
|
Infarction, Middle Cerebral Artery
|
Erectile Dysfunction
|
Kidney Neoplasms
|
Hyperinsulinism
|
Diabetic Retinopathy
|
Uterine Fibroid
|
Respiratory Distress Syndrome, Adult
|
Nervous System Malformations
|
Epilepsy, Temporal Lobe
|
Tongue Neoplasms
|
Meningioma
|
Developmental Disabilities
|
Nephrosis
|
Retinal Degeneration
|
Dermatitis, Allergic Contact
|
Lung Injury
|
Inflammatory Bowel Disease
|
Hyperlipidemias
|
Heat Stroke
|
Systemic Scleroderma
|
Chloracne
|
Ventricular Dysfunction, Left
|
Colitis
|
Microcephaly
|
Hypothermia
|
Thrombosis
|
Lymphoma, T-Cell, Peripheral
|
Asbestosis
|
Osteochondrodysplasias
|
Atrial Fibrillation
|
Unipolar Depression
|
Down Syndrome
|
Papilloma
|
Micronuclei, Chromosome-Defective
|
Thrombocytopenia
|
Basal Cell Carcinoma
|
Paralysis
|
Hearing Loss
|
Copper-Overload Cirrhosis
|
Hemolytic-Uremic Syndrome
|
Marfan Syndrome
|
Limb Dystonia
|
Carcinoma, Ductal, Breast
|
Metabolism, Inborn Errors
|
Metabolic Syndrome X
|
Pancreatic Diseases
|
Skin Abnormalities
|
Adenocarcinoma Of Esophagus
|
Microsatellite Instability
|
Growth Disorders
|
Demyelinating Diseases
|
Arteriosclerosis
|
Chromosome Aberrations
|
Neurotoxicity Syndromes
|
Hernias, Diaphragmatic, Congenital
|
Creutzfeldt Jacob Disease
|
Hypercholesterolemia, Familial
|
Neurogenic Inflammation
|
Liver Diseases, Parasitic
|
Aortic Diseases
|
Gestational Diabetes
|
Primary Biliary Cirrhosis
|
Ventricular Dysfunction
|
Gliosis
|
Vasospasm, Intracranial
|
Urticaria
|
Adenomatous Polyposis Coli
|
Pulmonary Hypertension
|
Morphine Dependence
|
Urologic Neoplasms
|
Amyloidosis
|
Motor Neuron Disease
|
Brain Diseases
|
Left Ventricular Hypertrophy
|
Sepsis
|
Fetal Growth Retardation
|
Glucose Intolerance
|
Movement Disorder
|
Diabetic Neuropathies
|
Nephrotic Syndrome
|
Carcinoma, Small Cell
|
Adenoma
|
Adrenal Gland Neoplasms
|
Bradycardia
|
Leukemia, Promyelocytic, Acute
|
Basal Ganglia Diseases
|
Anemia
|
Prostatic Intraepithelial Neoplasia
|
Leukemia, Myeloid
|
Drug Hypersensitivity
|
Barrett's Esophagus
|
Lymphoma, Large-Cell, Anaplastic
|
Lymphoma, Follicular
|
Hearing Loss, Sensorineural
|
Pulmonary Emphysema
|
Sarcoma
|
Emphysema
|
Scrapie
|
Malaria
|
Brain Edema
|
Hepatitis
|
Respiratory Tract Diseases
|
Attention Deficit Hyperactivity Disorder
|
Acute Lung Injury
|
Reticulocytosis
|
Adrenoleukodystrophy
|
Lymphoma
|
Genomic Instability
|
Macular Degeneration, Age-Related, 1
|
Membranous Glomerulonephritis
|
Aortic Aneurysm
|
Focal Segmental Glomerulosclerosis
|
Melas Syndrome
|
Meningomyelocele
|
Cleft Lip
|
Metabolic Diseases
|
Methylmalonic Acidemia
|
Coloboma
|
Migraine Disorder
|
Mitochondrial Diseases
|
Hand Deformities, Congenital
|
Motor Skills Disorders
|
Mouth Diseases
|
Bronchiectasis
|
Multiple Organ Failure
|
Muscular Atrophy, Spinal
|
Heart Arrest
|
Aortic Valve Insufficiency
|
Myasthenia Gravis
|
Mycobacterium Infections, Nontuberculous
|
Amyloidosis, Familial Visceral
|
Myocardial Stunning
|
Hematologic Diseases
|
Hemolysis
|
Hemorrhage
|
Hepatic Encephalopathy
|
Coronary Heart Disease
|
Hepatitis, Autoimmune
|
Coronary Restenosis
|
Neoplasms, Second Primary
|
Neoplasms, Squamous Cell
|
Nephritis
|
Nephritis, Interstitial
|
Cardiac Arrhythmia
|
Nerve Sheath Neoplasms
|
Neuropathic Pain
|
Hereditary Autoinflammatory Diseases
|
Hernia, Diaphragmatic
|
Heroin Dependence
|
Noonan Syndrome
|
Carcinogenesis
|
Occupational Diseases
|
Oligospermia
|
Ophthalmoplegia, Chronic Progressive External
|
Optic Atrophy
|
Osteitis Deformans
|
Alcohol Dependence
|
Huntington Disease
|
Osteogenesis Imperfecta, Type 2a
|
Osteogenesis Imperfecta, Type 3
|
Osteogenesis Imperfecta, Type 4
|
Deafness
|
Adenocarcinoma, Clear Cell
|
Ovarian Cysts
|
Ovarian Epithelial Cancer
|
Panic Disorder
|
Death
|
Hypercalcemia
|
Hypercholesterolemia
|
Dermatitis
|
Carcinoma, Intraductal, Noninfiltrating
|
Hypermethioninemia
|
Peritoneal Neoplasms
|
Diabetes Complications
|
Plaque, Atherosclerotic
|
Hyperthyroidism
|
Hypertriglyceridemia
|
Pneumonia, Pneumococcal
|
Polycystic Kidney, Autosomal Dominant
|
Polydactyly
|
Psoriatic Arthritis
|
Polyomavirus Infections
|
Preeclampsia
|
Pregnancy Complications, Cardiovascular
|
Premature Birth
|
Dog Diseases
|
Idiopathic Pulmonary Fibrosis
|
Drug Eruptions
|
Pulmonary Edema
|
Dyskinesia, Drug-Induced
|
Renal Insufficiency
|
Retinal Detachment
|
Cone-Rod Dystrophy 2
|
Dystonic Disorders
|
Intestinal Neoplasms
|
Asphyxia Neonatorum
|
Salivary Gland Neoplasm
|
Iron Metabolism Disorders
|
Sarcoma, Synovial
|
Ischemic Attack, Transient
|
Schistosomiasis
|
Ataxia
|
Ehlers-Danlos Syndrome, Type Vii, Autosomal Dominant
|
Juvenile Polyposis Syndrome
|
Abnormalities, Multiple
|
Sexual Dysfunctions, Psychological
|
Kidney Stone
|
Sjogren Syndrome
|
Eosinophilia
|
Soft Tissue Neoplasms
|
Solitary Fibrous Tumors
|
Cardiomyopathy, Hypertrophic, Familial
|
Atrophy
|
Language Development Disorders
|
Attention Deficit And Disruptive Behavior Disorders
|
Spinal Cord Injuries
|
Muscular Atrophy, Spinal, Infantile Chronic Form
|
Carotid Artery Diseases
|
Lead Poisoning
|
Splenomegaly
|
Carotid Artery Thrombosis
|
Leopard Syndrome
|
Autoimmune Lymphoproliferative Syndrome
|
Esophagitis
|
Anemia, Iron-Deficiency
|
Azoospermia
|
Facies
|
Tachycardia, Ventricular
|
Sickle Cell Anemia
|
Telomeric 22q13 Monosomy Syndrome
|
Bardet-Biedl Syndrome
|
Leukemia, Monocytic, Acute
|
Thrombasthenia
|
Thyroid Cancer, Follicular
|
Thyroid Cancer, Papillary
|
Aneurysm, Dissecting
|
Nicotine Dependence
|
Female Urogenital Diseases
|
Li-Fraumeni Syndrome
|
Cerebral Amyloid Angiopathy
|
Berylliosis
|
Beta-Thalassemia
|
Turner Syndrome
|
Lipodystrophy, Familial Partial
|
Urinary Bladder Diseases
|
Uterine Neoplasms
|
Angina, Stable
|
Ceroid Lipofuscinosis, Neuronal, 6
|
Fragile X Syndrome
|
Liver Failure
|
Long Qt Syndrome
|
Amino Acid Metabolism, Inborn Errors
|
Wounds And Injuries
|
Gait Disorders, Neurologic
|
Neural Tube Defects
|
Neurilemmoma
|
Neurocognitive Disorders
|
Neuroectodermal Tumors, Primitive
|
Neuroendocrine Tumors
|
Neuroferritinopathy
|
Neurologic Manifestations
|
Neuromyelitis Optica
|
Neuronopathy, Distal Hereditary Motor, Type Iib
|
Neuropathy, Distal Hereditary Motor, Type Iia
|
Neutropenia, Severe Congenital, X-Linked
|
Noonan Syndrome 5
|
Nystagmus, Congenital
|
Obesity, Morbid
|
Hypertelorism With Esophageal Abnormality And Hypospadias
|
Optic Atrophy Polyneuropathy Deafness
|
Organophosphate Poisoning
|
Orofaciodigital Syndrome Type1
|
Osteoarthritis With Mild Chondrodysplasia
|
Osteogenesis Imperfecta
|
Osteoglophonic Dwarfism
|
Osteolysis
|
Osteoporosis, Postmenopausal
|
Oto-Palato-Digital Syndrome Type 1
|
Overweight
|
Panniculitis, Nodular Nonsuppurative
|
Papilloma, Choroid Plexus
|
Papillomavirus Infections
|
Papillon-Lefevre Disease
|
Paresis
|
Paresthesia
|
Parkinson Disease 4, Autosomal Dominant Lewy Body
|
Parkinson Disease 7, Autosomal Recessive Early-Onset
|
Parkinson Disease, Secondary
|
Pediatric Obesity
|
Penile Neoplasms
|
Pentosuria
|
Periodontal Diseases
|
Periodontitis
|
Peripheral Demyelinating Neuropathy, Central Dysmyelination, Waardenburg Syndrome, And Hirschsprung Disease
|
Peripheral Nerve Injuries
|
Peripheral Vascular Diseases
|
Perisylvian Syndrome
|
Peters Anomaly
|
Pfeiffer Type Acrocephalosyndactyly
|
Phagocyte Bactericidal Dysfunction
|
Phosphoribosylpyrophosphate Synthetase Superactivity
|
Photophobia
|
Pitt-Hopkins Syndrome
|
Pituitary Acth Hypersecretion
|
Pituitary Diseases
|
Pituitary Neoplasms
|
Placenta Diseases
|
Plaque, Amyloid
|
Plasma Cell Granuloma, Pulmonary
|
Platyspondylic Lethal Skeletal Dysplasia, Torrance Type
|
Pleural Effusion
|
Pleurisy
|
Polycystic Kidney, Autosomal Recessive
|
Polycystic Lipomembranous Osteodysplasia With Sclerosing Leukoencephalopathy
|
Polycythemia
|
Polycythemia, Primary Familial And Congenital
|
Polyendocrinopathies, Autoimmune
|
Polymorphic Catecholergic Ventricular Tachycardia
|
Polymyositis
|
Porphyrias
|
Porphyrias, Hepatic
|
Postoperative Complications
|
Precocious Puberty, Central
|
Precursor B-Cell Lymphoblastic Leukemia-Lymphoma
|
Precursor T-Cell Lymphoblastic Leukemia-Lymphoma
|
Primary Lateral Sclerosis Juvenile
|
Primary Ovarian Insufficiency
|
Primary Ovarian Insufficiency, Fragile X-Associated
|
Prion Disease
|
Progeria
|
Progressive External Ophthalmoplegia With Mitochondrial Dna Deletions, Autosomal Dominant, 4
|
Propping Zerres Syndrome
|
Prostate Cancer, Familial
|
Protein Deficiency
|
Proteus Syndrome
|
Puberty, Delayed
|
Pulmonary Embolism
|
Q Fever
|
Radiation Injuries
|
Rapp-Hodgkin Syndrome
|
Raynaud Disease
|
Rectum Cancer
|
Respiratory Hypersensitivity
|
Respiratory Insufficiency
|
Respiratory System Abnormalities
|
Respiratory Tract Infections
|
Retinal Vein Occlusion
|
Retinitis Pigmentosa 18
|
Retinitis Pigmentosa 33
|
Retinitis Pigmentosa 42
|
Retinoblastoma
|
Rhabdomyolysis
|
Rhabdomyosarcoma
|
Rhabdomyosarcoma, Alveolar
|
Rhinitis, Allergic, Perennial
|
Ribose 5-Phosphate Isomerase Deficiency
|
Ring Dermoid Of Cornea
|
Rolandic Epilepsy, Mental Retardation, And Speech Dyspraxia, X-Linked
|
Sarcoidosis
|
Ewing Sarcoma
|
Sarcoma Family Syndrome Of Li And Fraumeni
|
Scapuloperoneal Syndrome, Neurogenic, Kaeser Type
|
Schistosomiasis Mansoni
|
Schizophrenia, Paranoid
|
Sciatic Neuropathy
|
Scleroderma, Localized
|
Sea-Blue Histiocyte Syndrome
|
Senior-Loken Syndrome 6
|
Serum Sickness
|
Sesame Syndrome
|
Severe Combined Immunodeficiency
|
Shock, Cardiogenic
|
Shock, Hemorrhagic
|
Septic Shock
|
Short Qt Syndrome 1
|
Short Qt Syndrome 3
|
Sick Sinus Syndrome
|
Sick Sinus Syndrome 2, Autosomal Dominant
|
Simpson-Golabi-Behmel Syndrome, Type 2
|
Skeletal Defects, Genital Hypoplasia, And Mental Retardation
|
Sleep Apnea Syndromes
|
Insomnia
|
Spasm
|
Spastic Paraplegia 3, Autosomal Dominant
|
Spherocytosis, Hereditary
|
Spina Bifida Cystica
|
Spinal Cord Compression
|
Spinal Cord Diseases
|
Spinal Muscular Atrophy 4
|
Spinocerebellar Ataxia 10
|
Spinocerebellar Ataxia 17
|
Spinocerebellar Ataxia, Autosomal Recessive 1
|
Spinocerebellar Ataxia, Autosomal Recessive 8
|
Spinocerebellar Ataxias
|
Split-Hand-Foot Malformation 4
|
Ankylosing Spondylitis
|
Spondylocarpotarsal Synostosis
|
Spondyloepiphyseal Dysplasia, Congenita
|
Spondylometaphyseal Dysplasia, Kozlowski Type
|
Spongiform Encephalopathy With Neuropsychiatric Features
|
Starvation
|
Stickler Syndrome, Type 1
|
Stickler Syndrome, Type I, Nonsyndromic Ocular
|
Stomach Diseases
|
Stomatognathic Diseases
|
Strudwick Syndrome
|
Progressive Supranuclear Palsy
|
Surfactant Metabolism Dysfunction, Pulmonary, 1
|
Surfactant Metabolism Dysfunction, Pulmonary, 2
|
Sweat Gland Neoplasms
|
Synovitis
|
Synpolydactyly 2
|
Tachycardia, Sinus
|
Tarp Syndrome
|
Taste Disorders
|
Temple-Baraitser Syndrome
|
Testicular Germ Cell Tumor
|
Tetralogy Of Fallot
|
Thiamine Deficiency
|
Thrombocythemia, Essential
|
Thrombocytopenia 1
|
Thrombocytopenia, Neonatal Alloimmune
|
Thrombotic Microangiopathies
|
Thymoma
|
Thymus Neoplasms
|
Thyroid Carcinoma, Anaplastic
|
Tic Disorders
|
Toenail Dystrophy, Isolated
|
Tooth Abnormalities
|
Torsades De Pointes
|
Transient Bullous Dermolysis Of The Newborn
|
Tremor
|
Trismus
|
Tuberculosis
|
Uremia
|
Ureteral Calculi
|
Urogenital Neoplasms
|
Vacterl Association With Hydrocephalus
|
Vanishing White Matter Leukodystrophy With Ovarian Failure
|
Vascular System Injuries
|
Vasculitis
|
Venous Thromboembolism
|
Ventricular Fibrillation
|
Ventricular Outflow Obstruction
|
Ventricular Remodeling
|
Vesicoureteral Reflux 2
|
Vitamin A Deficiency
|
Best Vitelliform Macular Dystrophy, Multifocal
|
Vitreoretinochoroidopathy
|
Von Willebrand Disease, Type 1
|
Von Willebrand Disease, Type 2
|
Von Willebrand Disease, Type 3
|
Vulvar Lichen Sclerosus
|
Waardenburg Syndrome Type 2
|
Waardenburg Syndrome, Type 4c
|
Wallerian Degeneration
|
Wiskott-Aldrich Syndrome
|
Wolcott-Rallison Syndrome
|
Wounds, Penetrating
|
Yellow Nail Syndrome
|
Yemenite Deaf-Blind Hypopigmentation Syndrome
|
Zimmerman Laband Syndrome
|
Iridogoniodysgenesis, Dominant Type
|
6-Pyruvoyl-Tetrahydropterin Synthase Deficiency
|
Aberrant Crypt Foci
|
Abortion, Threatened
|
Achondrogenesis Type 2
|
Acidosis, Lactic
|
Acromesomelic Dysplasia, Maroteaux Type
|
Adenoma, Liver Cell
|
Adrenocortical Carcinoma, Hereditary
|
Agammaglobulinemia
|
Aggressive Periodontitis
|
Aging, Premature
|
Aids-Related Kaposi Sarcoma
|
Alexander Disease
|
Alkaptonuria
|
Androgenetic Alopecia
|
Alpha 1-Antitrypsin Deficiency
|
Alpha-B Crystallinopathy
|
Alveolitis, Extrinsic Allergic
|
Alzheimer Disease Type 2
|
Ameloblastoma
|
Amelogenesis Imperfecta, Hypomaturation Type, With Snow-Capped Teeth
|
Aminoacylase 1 Deficiency
|
Amnesia
|
Amyloid Neuropathies, Familial
|
Amyloidosis, Familial
|
Amyloidosis, Hereditary, Transthyretin-Related
|
Amyotrophic Lateral Sclerosis 10
|
Amyotrophic Lateral Sclerosis 2, Juvenile
|
Amyotrophic Lateral Sclerosis 4, Juvenile
|
Amyotrophic Lateral Sclerosis 6, Autosomal Recessive
|
Andersen Syndrome
|
Anemia, Hemolytic
|
Anemia, Hemolytic, Congenital Nonspherocytic
|
Anemia, Hypoplastic, Congenital
|
Anemia, Refractory
|
Anemia, Sideroblastic
|
Angioedema
|
Anisometropia
|
Anorexia
|
Anthracosis
|
Anuria
|
Anxiety, Separation
|
Thoracic Aortic Aneurysm
|
Aortic Rupture
|
Aphasia
|
Apnea
|
Arenaviridae Infections
|
Argininosuccinic Aciduria
|
Arrhythmogenic Right Ventricular Dysplasia, Familial, 1
|
Arrhythmogenic Right Ventricular Dysplasia, Familial, 2
|
Arthralgia
|
Arthritis
|
Arthritis, Infectious
|
Arts Syndrome
|
Asthma, Occupational
|
Ataxia With Vitamin E Deficiency
|
Atelosteogenesis, Type 1
|
Athabaskan Brainstem Dysgenesis
|
Autoimmune Polyendocrinopathy Syndrome, Type 1
|
Balkan Nephropathy
|
Bamforth Syndrome
|
Behcet's Syndrome
|
Bernard-Soulier Syndrome
|
Bile Duct Neoplasms
|
Bone Diseases, Developmental
|
Bone Diseases, Metabolic
|
Bone Neoplasms
|
Boomerang Dysplasia
|
Brachydactyly
|
Brachydactyly Type A2
|
Brachydactyly Type C
|
Brain Diseases, Metabolic, Inborn
|
Brain Infarction
|
Breast Diseases
|
Breast Neoplasms, Male
|
Bronchial Hyperreactivity
|
Chronic Bronchitis
|
Brugada Syndrome 8
|
Bruton Type Agammaglobulinemia
|
Burns
|
Butyrylcholinesterase Deficiency
|
Cachexia
|
Cadmium Poisoning
|
Candidiasis
|
Candidiasis, Chronic Mucocutaneous
|
Cantu Syndrome
|
Carcinoma, Ductal
|
Sudden Cardiac Arrest
|
Deficiency Diseases
|
Dementia
|
Carcinoma, Large Cell
|
Carcinoma, Pancreatic Ductal
|
Carcinosarcoma
|
Cardiofaciocutaneous Syndrome
|
Cardiomyopathy, Dilated, 1aa
|
Cardiomyopathy, Dilated, 1ee
|
Cardiomyopathy, Dilated, 1g
|
Cardiomyopathy, Dilated, 1i
|
Cardiomyopathy, Dilated, 1o
|
Cardiomyopathy, Dilated, 1p
|
Cardiomyopathy, Familial Hypertrophic, 1
|
Cardiomyopathy, Familial Hypertrophic, 14
|
Cardiomyopathy, Familial Hypertrophic, 4
|
Cardiomyopathy, Familial Hypertrophic, 9
|
Cardiotoxicity
|
Cardiovascular Abnormalities
|
Cardiovirus Infections
|
Carnitine Palmitoyl Transferase 1a Deficiency
|
Carotid Intimal Medial Thickness 1
|
Carotid Stenosis
|
Carpal Tunnel Syndrome
|
Cataract And Cardiomyopathy
|
Cataract, Coppock-Like
|
Cataract, Posterior Polar, 3
|
Cataract, Zonular Pulverulent 3
|
Caudal Duplication Anomaly
|
Cecal Neoplasms
|
Celiac Disease
|
Central Nervous System Diseases
|
Central Nervous System Neoplasms
|
Cerebellar Diseases
|
Cerebral Amyloid Angiopathy, App-Related
|
Cerebral Amyloid Angiopathy, Familial
|
Cerebral Hemorrhage With Amyloidosis, Hereditary, Dutch Type
|
Cerulean Cataract
|
Charcot-Marie-Tooth Disease, Type 1f
|
Charcot-Marie-Tooth Disease, Type 2e
|
Charcot-Marie-Tooth Disease, Type 2f
|
Chilblain Lupus 1
|
Child Development Disorders, Pervasive
|
Chlamydia Infections
|
Cholangitis
|
Chondrodysplasia, Grebe Type
|
Chondrosarcoma
|
Chondrosarcoma, Extraskeletal Myxoid
|
Chondrosarcoma, Mesenchymal
|
Choroidal Neovascularization
|
Chromosome 17 Deletion
|
Chronobiology Disorders
|
Chudley-Mccullough Syndrome
|
Citrullinemia
|
Clear-Cell Metastatic Renal Cell Carcinoma
|
Color Vision Defects
|
Coma
|
Congenital Abnormalities
|
Conjunctival Diseases
|
Constipation
|
Coproporphyria, Hereditary
|
Corneal Neovascularization
|
Coronary Artery Disease, Autosomal Dominant 2
|
Coronary Thrombosis
|
Corpus Callosum, Partial Agenesis Of, X-Linked
|
Costello Syndrome
|
Craniopharyngioma
|
Craniosynostoses
|
Cryptorchidism
|
Cushing's Symphalangism
|
Cutis Laxa
|
Cutis Laxa, Autosomal Recessive, Type Iib
|
Cystitis
|
Cytomegalovirus Infection
|
Deafness, Autosomal Dominant 1
|
Deafness, Autosomal Dominant 20
|
Deafness, Autosomal Recessive 39
|
Deafness, X-Linked 1
|
Major Depression
|
Atopic Eczema
|
Dermatitis, Occupational
|
Dermatomyositis
|
Diabetes Mellitus, Insulin-Dependent, 2
|
Diabetes Mellitus, Permanent Neonatal
|
Diabetic Ketoacidosis
|
Disease Susceptibility
|
Disorders Of Sex Development
|
Disruptive, Impulse Control, And Conduct Disorders
|
Distal Myopathies
|
Ductus Arteriosus, Patent
|
Dwarfism
|
Dyskinesias
|
Dysostoses
|
Dystonia 6, Torsion
|
Dystransthyretinemic Euthyroidal Hyperthyroxinemia
|
Echinococcosis
|
Ectodermal Dysplasia, Anhidrotic, With T-Cell Immunodeficiency, Autosomal Dominant
|
Ectrodactyly-Cleft Lip-Palate Syndrome
|
Ectrodactyly, Ectodermal Dysplasia, And Cleft Lip-Palate Syndrome 3
|
Ehlers-Danlos Syndrome, Cardiac Valvular Form
|
Ehlers-Danlos Syndrome Type 1
|
Encephalitis, Herpes Simplex
|
Encephalomyelitis, Autoimmune, Experimental
|
Endometrial Hyperplasia
|
Endotoxemia
|
Enterocolitis
|
Ependymoma
|
Epidermolysis Bullosa Dystrophica
|
Epidermolysis Bullosa Dystrophica, Pasini Type
|
Epidermolysis Bullosa, Pretibial
|
Epidermolysis Bullosa Pruriginosa
|
Epidermolysis Bullosa With Congenital Localized Absence Of Skin And Deformity Of Nails
|
Epilepsies, Myoclonic
|
Epilepsy, Tonic-Clonic
|
Epileptic Encephalopathy, Early Infantile, 1
|
Epileptic Encephalopathy, Early Infantile, 4
|
Epiphyseal Dysplasia, Multiple, With Myopia And Conductive Deafness
|
Erythema
|
Esophageal Diseases
|
Esophageal Stenosis
|
Exanthema
|
Eye Abnormalities
|
Eye Diseases, Hereditary
|
Familial Dilated Cardiomyopathy
|
Familial Testotoxicosis
|
Fanconi Anemia
|
Farber Lipogranulomatosis
|
Fasciculation
|
Fatty Liver, Alcoholic
|
Favism
|
Feminization
|
Femur Head Necrosis
|
Fibroma
|
Fibromatosis, Aggressive
|
Fibular Hypoplasia And Complex Brachydactyly
|
Flushing
|
Foot Deformities, Congenital
|
Fragile X Tremor Ataxia Syndrome
|
Frontotemporal Lobar Degeneration
|
Fructose-1,6-Diphosphatase Deficiency
|
Fructose Intolerance
|
Galactosemias
|
Cystathionase Deficiency
|
Gastrointestinal Neoplasms
|
Gaucher Disease
|
Amyloidosis, Cerebral, With Spongiform Encephalopathy
|
Gingival Hyperplasia
|
Open-Angle Glaucoma
|
Glaucoma, Primary Open Angle
|
Gliosarcoma
|
Iga Glomerulonephritis
|
Glomerulonephritis, Membranoproliferative
|
Glomerulopathy With Fibronectin Deposits
|
Glucosephosphate Dehydrogenase Deficiency
|
Glut1 Deficiency Syndrome
|
Glutamine Deficiency, Congenital
|
Glutathione Synthetase Deficiency
|
Glutathione Synthetase Deficiency Of Erythrocytes, Hemolytic Anemia Due To
|
Glycogen Storage Disease Type Vii
|
Glycogen Storage Disease Xii
|
Gonadal Dysgenesis
|
Gout, Hprt-Related
|
Granuloma, Plasma Cell
|
Granuloma, Respiratory Tract
|
Granulomatous Disease, Chronic
|
Growth Mental Deficiency Syndrome Of Myhre
|
Hallucinations
|
Hamartoma Syndrome, Multiple
|
Hashimoto Disease
|
Hay-Wells Syndrome
|
Heartburn
|
Heart Injuries
|
Heart Septal Defects, Atrial
|
Helicobacter Infections
|
Hemangioma
|
Hematoma
|
Hemochromatosis
|
Hepatitis, Alcoholic
|
Hepatitis C
|
Hepatoblastoma
|
Hepatomegaly
|
Hereditary Angioedema Types I And Ii
|
Hereditary Macular Coloboma
|
Hereditary Myopathy With Early Respiratory Failure
|
Hereditary Spastic Paralysis, Infantile Onset Ascending
|
Heredodegenerative Disorders, Nervous System
|
Hip Fractures
|
Hirschsprung Disease
|
Histiocytoma, Angiomatoid Fibrous
|
Hiv Seropositivity
|
Hiv Wasting Syndrome
|
Hodgkins Lymphoma
|
Homocystinuria
|
Huntington Disease-Like 1
|
Hyaloideoretinal Degeneration Of Wagner
|
Hydrocephalus, X-Linked
|
Hydroxyacyl-Coa Dehydrogenase, Type 2, Deficiency
|
Hyperammonemia
|
Hyperbilirubinemia
|
Hyperemia
|
Hyperferritinemia, Hereditary, With Congenital Cataracts
|
Hypergammaglobulinemia
|
Hyper-Ige Recurrent Infection Syndrome, Autosomal Dominant
|
Hyperinsulinemic Hypoglycemia, Familial, 6
|
Hyperkalemia
|
Hyperlipoproteinemia Type Iii
|
Hyperostosis, Cortical, Congenital
|
Hyperoxaluria
|
Hyperphagia
|
Hyperprolactinemia
|
Hyperprolinemia Type 2
|
Hypersensitivity, Delayed
|
Hypersplenism
|
Hypertension, Portal
|
Hyperthyroxinemia, Familial Dysalbuminemic
|
Hyperuricemia
|
Hypoalbuminemia
|
Familial Hdl Deficiency
|
Hypogammaglobulinemia And Isolated Growth Hormone Deficiency, X-Linked
|
Hypogonadism
|
Hypokalemia
|
Hypomagnesemia 5, Renal, With Ocular Involvement
|
Hypomagnesemia Primary
|
Hypoproteinemia, Hypercatabolic
|
Hypospadias
|
Hypoxia-Ischemia, Brain
|
Ichthyosis, Leukocyte Vacuoles, Alopecia, And Sclerosing Cholangitis
|
Idiopathic Basal Ganglia Calcification 1
|
Idiopathic Hypogonadotropic Hypogonadism
|
Iga Deficiency
|
Immune Dysfunction With T-Cell Inactivation Due To Calcium Entry Defect 1
|
Immune Dysfunction With T-Cell Inactivation Due To Calcium Entry Defect 2
|
Immunoblastic Lymphadenopathy
|
Immunodeficiency Due To Defect In Cd3-Zeta
|
Immunologic Deficiency Syndromes
|
Inclusion Body Myopathy With Early-Onset Paget Disease And Frontotemporal Dementia
|
Infection
|
Infertility
|
Inflammatory Bowel Disease 10
|
Inflammatory Breast Neoplasms
|
Insomnia, Fatal Familial
|
Insulin-Like Growth Factor I, Resistance To
|
Intervertebral Disc Disease
|
Intestinal Polyps
|
Intracranial Thrombosis
|
Intrahepatic Cholestasis Of Pregnancy
|
46, Xy Disorders Of Sex Development
|
Jackson-Weiss Syndrome
|
Job Syndrome
|
Joubert Syndrome 10
|
Joubert Syndrome 3
|
Joubert Syndrome 5
|
Juvenile-Onset Dystonia
|
Juvenile Polyposis With Hereditary Hemorrhagic Telangiectasia
|
Kallmann Syndrome
|
Keratosis
|
Keratosis Palmoplantaris With Periodontopathia And Onychogryposis
|
Kidney Diseases, Cystic
|
Kidney Tubular Necrosis, Acute
|
Kniest Dysplasia
|
Knobloch Syndrome
|
Kyphosis
|
Lactate Dehydrogenase Deficiency Type A
|
Lactose Intolerance, Adult Type
|
Lameness, Animal
|
Language Disorders
|
Larsen Syndrome
|
Late-Onset Retinal Degeneration
|
Laurin-Sandrow Syndrome
|
Lead Poisoning, Nervous System
|
Leber Congenital Amaurosis
|
Leber Congenital Amaurosis 10
|
Legg-Calve-Perthes Disease
|
Leishmaniasis
|
Leishmaniasis, Cutaneous
|
Visceral Leishmaniasis
|
Lens Diseases
|
Leopard Syndrome, 2
|
Leprosy
|
Lesch-Nyhan Syndrome
|
Lethal Arthrogryposis With Anterior Horn Cell Disease
|
Lethal Congenital Contracture Syndrome 1
|
Lethal Congenital Contracture Syndrome 2
|
Leukemia, Erythroblastic, Acute
|
Leukemia, Lymphoid
|
Leukemia, Megakaryoblastic, Acute
|
Leukemia, Megakaryoblastic, Of Down Syndrome
|
Chronic Myelogenous Leukemia
|
Leukemia, Myelomonocytic, Acute
|
Leukemia, Myelomonocytic, Juvenile
|
Leukemia, T-Cell
|
Leukostasis
|
Leydig Cell Hypoplasia
|
Leydig Cell Tumor
|
Li-Fraumeni Syndrome 2
|
Limb Deformities, Congenital
|
Limb-Girdle Muscular Dystrophy Type 2h
|
Limb-Mammary Syndrome
|
Lipidoses
|
Lipodystrophy, Congenital Generalized, Type 3
|
Lipomatosis
|
Lipoprotein Glomerulopathy
|
Liposarcoma
|
Liposarcoma, Myxoid
|
Listeriosis
|
Furlong Syndrome
|
Long Qt Syndrome 2
|
Interstitial Lung Disease
|
Polyploidy
|
Porokeratosis, Disseminated Superficial Actinic 1
|
Porphyria, Acute Hepatic
|
Lupus Nephritis
|
Lymphedema Distichiasis Syndrome
|
Lymphedema, Hereditary, Ii
|
Lymphoproliferative Syndrome, X-Linked, 2
|
Machado-Joseph Disease
|
Macrocephaly Autism Syndrome
|
Macrophage Activation Syndrome
|
Macular Degeneration, Age-Related, 11
|
Macular Dystrophy, Concentric Annular
|
Macular Edema
|
Malaria, Falciparum
|
Malnutrition
|
Mandibular Neoplasms
|
Mandibuloacral Dysplasia With Type A Lipodystrophy
|
Marijuana Dependence
|
Masa (Mental Retardation, Aphasia, Shuffling Gait, Adducted Thumbs) Syndrome
|
Maturity-Onset Diabetes Of The Young, Type 1
|
Meckel Syndrome, Type 4
|
Medium Chain Acyl Coa Dehydrogenase Deficiency
|
Megaepiphyseal Dwarfism
|
Meningioma, Familial
|
Meningitis, Aseptic
|
Mental Retardation, Autosomal Recessive 6
|
Mental Retardation, X-Linked
|
Mental Retardation, X-Linked 17
|
Mental Retardation, X-Linked, Syndromic 10
|
Mental Retardation, X-Linked, Syndromic, Jarid1c-Related
|
Mercury Poisoning
|
Mercury Poisoning, Nervous System
|
Metaphyseal Anadysplasia 2
|
Metaplasia
|
Mevalonate Kinase Deficiency
|
Microcephaly, Primary Autosomal Recessive, 1
|
Migraine Without Aura
|
Mild Cognitive Impairment
|
Mitochondrial Encephalomyopathies
|
Mitochondrial Myopathies
|
Molybdenum Cofactor Deficiency
|
Mosaic Variegated Aneuploidy Syndrome
|
Multiple Chemical Sensitivity
|
Multiple Sclerosis, Relapsing-Remitting
|
Multiple Synostoses Syndrome 2
|
Muscle Weakness
|
Muscular Dystrophies
|
Muscular Dystrophy, Emery-Dreifuss
|
Muscular Dystrophy, Limb-Girdle, Type 2j
|
Musculoskeletal Abnormalities
|
Musculoskeletal Pain
|
Myasthenic Syndrome, Congenital, Type Id
|
Mycobacterium Infections
|
Myd88 Deficiency
|
Myelodysplastic Syndromes
|
Myeloproliferative Disorder
|
Myocarditis
|
Myoclonic Dystonia
|
Myoclonic Epilepsies, Progressive
|
Myoglobinuria
|
Myopathies, Structural, Congenital
|
Myopathy, Early-Onset, With Fatal Cardiomyopathy
|
Myopia
|
Myostatin-Related Muscle Hypertrophy
|
Nasopharyngeal Neoplasm
|
Nausea
|
Neointima
|
Porphyria Cutanea Tarda
|
Neoplasms, Bone Tissue
|
Neovascularization, Pathologic
|
Nephrogenic Fibrosing Dermopathy
|