Breast Carcinoma
|
Liver Cirrhosis, Experimental
|
Craniofacial Abnormalities
|
Prostatic Neoplasms
|
Stomach Neoplasms
|
Lung Neoplasms
|
Carcinoma, Non-Small-Cell Lung
|
Neoplasm Metastasis
|
Colorectal Cancer
|
Hepatocellular Carcinoma
|
Colonic Neoplasm
|
Pancreatic Carcinoma
|
Cell Transformation, Neoplastic
|
Carcinoma
|
Hernia, Diaphragmatic
|
Squamous Cell Carcinoma
|
Skin Neoplasms
|
Glioblastoma Multiforme
|
Diabetes Mellitus, Type 2
|
Hypertension
|
Neoplasm Invasiveness
|
Adenocarcinoma
|
Urinary Bladder Neoplasms
|
Glioma
|
Ovarian Neoplasms
|
Drug-Induced Liver Injury
|
Autism
|
Neoplasms
|
Astrocytoma
|
Autism Spectrum Disorder
|
Disease Progression
|
Liver Neoplasms, Experimental
|
Esophageal Squamous Cell Carcinoma
|
Osteosarcoma
|
Endometrial Neoplasm
|
Endometriosis
|
Diabetes Mellitus, Experimental
|
Hemangiosarcoma
|
Mammary Neoplasms, Experimental
|
Esophageal Neoplasms
|
Myocardial Ischemia
|
Uterine Cervical Neoplasms
|
Rheumatoid Arthritis
|
Brain Neoplasms
|
Mesothelioma, Malignant
|
Carcinoma, Adenoid Cystic
|
Heart Defects, Congenital
|
Schizophrenia
|
Cleft Lip
|
Liver Cirrhosis
|
Heart Failure
|
Mammary Neoplasms, Animal
|
Erectile Dysfunction
|
Skin Diseases
|
Renal Cell Carcinoma
|
Adenoma
|
Reperfusion Injury
|
Cholangiocarcinoma
|
Asthma
|
Fatty Liver
|
Disease Models, Animal
|
Sezary Syndrome
|
Myocardial Infarction
|
Acute Kidney Injury
|
Amyotrophic Lateral Sclerosis 1
|
Small Cell Lung Carcinoma
|
Liver Neoplasms
|
Myocardial Reperfusion Injury
|
Lung Diseases
|
Male Infertility
|
Inflammation
|
Calcinosis
|
Tetralogy Of Fallot
|
Basal Cell Carcinoma
|
Tooth Abnormalities
|
Neuroectodermal Tumors, Primitive
|
Medulloblastoma
|
Atrial Fibrillation
|
Melanoma
|
Cardiomyopathies
|
Cardiomyopathy, Hypertrophic
|
Mesothelioma
|
Carcinoma, Pancreatic Ductal
|
Craniosynostoses
|
Arthritis, Juvenile
|
Lung Adenocarcinoma
|
Neoplasm Recurrence, Local
|
Sarcoma
|
Dilated Cardiomyopathy
|
Infertility, Female
|
Aneurysm, Dissecting
|
Polycystic Ovary Syndrome
|
Leukemia-Lymphoma, Adult T-Cell
|
Peritoneal Neoplasms
|
Chloracne
|
Furlong Syndrome
|
Mouth Neoplasms
|
Burkitt Lymphoma
|
Diabetic Nephropathy
|
Seizures
|
Alzheimer's Disease
|
Hiv Infections
|
Leukemia, Myeloid, Acute
|
Osteoarthritis
|
Focal Segmental Glomerulosclerosis
|
Arsenic Poisoning
|
Ulcerative Colitis
|
Hyperlipidemias
|
Intellectual Disability
|
Adenocarcinoma Of Esophagus
|
Cardiovascular Disease
|
Cardiac Hypertrophy
|
Multiple Myeloma
|
Uremia
|
Gastrointestinal Diseases
|
Precancerous Conditions
|
Pulmonary Hypertension
|
Carcinoma, Small Cell
|
Heinz Body Anemias
|
Acute Lung Injury
|
Muscular Atrophy
|
Muscular Diseases
|
Carcinoma, Transitional Cell
|
Myelodysplastic Syndromes
|
Cryptorchidism
|
Hepatitis, Chronic
|
Nasopharyngeal Neoplasm
|
Deafness
|
Neoplasms, Experimental
|
Neovascularization, Pathologic
|
Basal Cell Nevus Syndrome
|
Nephrosis
|
Nerve Degeneration
|
Nervous System Diseases
|
Acrocephalosyndactylia
|
Neuroblastoma
|
Cyclopia
|
Alpha-Thalassemia
|
Aortic Aneurysm
|
Hyperalgesia
|
Hypercholesterolemia
|
Cardiomyopathy, Hypertrophic, Familial
|
Hyperglycemia
|
Hyperkeratosis, Epidermolytic
|
Hypertension, Essential
|
Hypertension, Portal
|
Bone Diseases
|
Bone Diseases, Developmental
|
Hypertrophy
|
Osteochondrodysplasias
|
Left Ventricular Hypertrophy
|
Abnormalities, Multiple
|
Cecal Neoplasms
|
Hypotension
|
Cardiac Arrhythmia
|
Idiopathic Hypogonadotropic Hypogonadism
|
Infarction, Middle Cerebral Artery
|
Peripheral Neuropathy
|
Pfeiffer Type Acrocephalosyndactyly
|
Influenza, Human
|
Insulin Resistance
|
Drug-Related Side Effects And Adverse Reactions
|
Polycystic Kidney, Autosomal Dominant
|
Polycystic Kidney Diseases
|
Adrenal Gland Neoplasms
|
Ischemia
|
Jackson-Weiss Syndrome
|
Polydactyly
|
Intracerebral Hemorrhage
|
Cerebral Infarction
|
Adrenocortical Carcinoma
|
Juvenile Polyposis Syndrome
|
Precursor B-Cell Lymphoblastic Leukemia-Lymphoma
|
Acute Lymphoblastic Leukemia
|
Precursor T-Cell Lymphoblastic Leukemia-Lymphoma
|
Preeclampsia
|
Kallmann Syndrome
|
Enterocolitis, Necrotizing
|
Keratosis
|
Prostatic Intraepithelial Neoplasia
|
Kidney Disease
|
Proteinuria
|
Psoriasis
|
Chronic Obstructive Pulmonary Disease
|
Epilepsy, Temporal Lobe
|
Respiratory Distress Syndrome, Adult
|
Respiratory System Abnormalities
|
Eye Abnormalities
|
Retinal Diseases
|
Rhabdomyosarcoma
|
Leukemia, Myeloid
|
Breast Neoplasms, Male
|
Leukemia, Promyelocytic, Acute
|
Scoliosis
|
Sepsis
|
Acute Coronary Syndrome
|
Limb Deformities, Congenital
|
Skin Abnormalities
|
Liver Diseases, Parasitic
|
Atherosclerosis
|
Spinal Dysraphism
|
Gallbladder Neoplasm
|
Status Epilepticus
|
Toxic Epidermal Necrolysis
|
Stomach Ulcer
|
Lymphangioleiomyomatosis
|
Lymphoma
|
Lymphoma, T-Cell
|
Lymphoma, T-Cell, Cutaneous
|
Carcinoma, Ductal, Breast
|
Thyroid Carcinoma
|
Colorectal Neoplasms, Hereditary Nonpolyposis
|
Congenital Abnormalities
|
Urologic Neoplasms
|
Meningioma
|
Aicardi-Goutieres Syndrome
|
Hamartoma Syndrome, Multiple
|
Ventricular Remodeling
|
Head And Neck Neoplasms
|
Coronary Artery Disease
|
Heart Valve Diseases
|
Language Development Disorders
|
Learning Disorders
|
Uterine Fibroid
|
Leukemia
|
Chronic Lymphocytic Leukemia
|
Leukemia, Lymphoid
|
Leukemia, Megakaryoblastic, Of Down Syndrome
|
Leukemia, Myeloid, Accelerated Phase
|
Leukemia, Myelomonocytic, Juvenile
|
Leukemia, T-Cell
|
Lewy Body Dementia
|
Li-Fraumeni Syndrome
|
Lig4 Syndrome
|
Alcoholic Liver Cirrhosis
|
Liver Diseases
|
Liver Failure
|
Lung Diseases, Obstructive
|
Systemic Lupus Erythematosus
|
Lymphatic Metastasis
|
Lymphoma, Follicular
|
Lymphoma, Large B-Cell, Diffuse
|
Lymphoma, Large-Cell, Anaplastic
|
Lymphoma, Mantle-Cell
|
Colorectal Cancer, Hereditary Nonpolyposis, Type 1
|
Macrothrombocytopenia Progressive Deafness
|
Age-Related Macular Degeneration
|
Macular Edema
|
Marfan Syndrome
|
Mastocytosis
|
Maxillary Neoplasms
|
Meckel Syndrome, Type 5
|
Medullary Cystic Kidney Disease 1
|
Megalencephaly
|
Memory Disorders
|
Menkes Kinky Hair Syndrome
|
Mental Disorders
|
Metabolic Diseases
|
Metabolic Syndrome X
|
Metaphyseal Dysplasia Without Hypotrichosis
|
Methemoglobinemia
|
Microcephalic Osteodysplastic Primordial Dwarfism, Type Ii
|
Microcephaly
|
Microcephaly, Primary Autosomal Recessive, 7
|
Microsatellite Instability
|
Migraine Disorder
|
Mitochondrial Encephalomyopathies
|
Motor Neuron Disease
|
Motor Skills Disorders
|
Muir-Torre Syndrome
|
Muscle Weakness
|
Muscular Dystrophy, Limb-Girdle, Type 2j
|
Mycoplasma Infections
|
Myeloproliferative Disorder, Chronic, With Eosinophilia
|
Myeloproliferative Disorder
|
Myh9-Related Disorders
|
Myopathy, Early-Onset, With Fatal Cardiomyopathy
|
Myopia
|
Myositis Ossificans
|
Myotonia
|
Nail-Patella Syndrome
|
Nasopharyngeal Carcinoma
|
Neointima
|
Neoplasms, Germ Cell And Embryonal
|
Alport Syndrome, X-Linked
|
Nerve Sheath Neoplasms
|
Neural Tube Defects
|
Neurodegenerative Diseases
|
Neurodevelopmental Disorders
|
Neuroectodermal Tumors
|
Neurofibromatosis 1
|
Neurologic Manifestations
|
Neurotoxicity Syndromes
|
Nijmegen Breakage Syndrome
|
Multiple Synostoses Syndrome 1
|
No-Reflow Phenomenon
|
Occipital Horn Syndrome
|
Occupational Diseases
|
Oculocerebrorenal Syndrome
|
Oculodentodigital Dysplasia
|
Oculodentodigital Dysplasia, Autosomal Recessive
|
Oculootoradial Syndrome
|
Oligodendroglioma
|
Oncocytoma, Renal
|
Optic Atrophies, Hereditary
|
Optic Atrophy, Hereditary, Leber
|
Oral Ulcer
|
Orofacial Cleft 5
|
Orofaciodigital Syndromes
|
Osler-Rendu-Weber Syndrome 2
|
Osteoglophonic Dwarfism
|
Osteoporosis
|
Ovarian Cysts
|
Ovarian Epithelial Cancer
|
Pain
|
Pallister-Hall Syndrome
|
Papilloma, Choroid Plexus
|
Paralysis
|
Parkinson's Disease
|
Penile Neoplasms
|
Peptic Ulcer
|
Peripheral Arterial Disease
|
Peripheral Demyelinating Neuropathy, Central Dysmyelination, Waardenburg Syndrome, And Hirschsprung Disease
|
Peritonitis
|
Peters Anomaly
|
Phyllodes Tumor
|
Pilomatrixoma
|
Plagiocephaly, Nonsynostotic
|
Platelet Disorder, Familial, With Associated Myeloid Malignancy
|
Pneumothorax
|
Pneumothorax, Primary Spontaneous
|
Poisoning
|
Polycystic Liver Disease
|
Polycythemia
|
Polycythemia Vera
|
Polydactyly, Postaxial
|
Polydactyly, Preaxial 4
|
Polyploidy
|
Polyposis Syndrome, Hereditary Mixed, 2
|
Posterior Column Ataxia With Retinitis Pigmentosa
|
Premature Birth
|
Prenatal Injuries
|
Primary Lateral Sclerosis Juvenile
|
Progressive External Ophthalmoplegia With Mitochondrial Dna Deletions, Autosomal Dominant, 4
|
Prostate Cancer, Familial
|
Prostatic Neoplasms, Castration-Resistant
|
Pulmonary Alveolar Microlithiasis
|
Pulmonary Edema
|
Pulmonary Fibrosis
|
Recurrence
|
Renal Insufficiency
|
Respiratory Hypersensitivity
|
Retinal Degeneration
|
Retinal Vein Occlusion
|
Rhabdoid Tumor Predisposition Syndrome 2
|
Ring Dermoid Of Cornea
|
Saethre-Chotzen Syndrome With Eyelid Anomalies
|
Salivary Gland Neoplasm
|
Sarcoma Family Syndrome Of Li And Fraumeni
|
Sarcoma, Synovial
|
Scaphocephaly, Maxillary Retrusion, And Mental Retardation
|
Sciatic Neuropathy
|
Seckel Syndrome 1
|
Seckel Syndrome 2
|
Severe Combined Immunodeficiency Due To Adenosine Deaminase Deficiency
|
Sick Sinus Syndrome
|
Sick Sinus Syndrome 2, Autosomal Dominant
|
Silver-Russell Syndrome
|
Sjogren Syndrome
|
Obstructive Sleep Apnea
|
Insomnia
|
Spasms, Infantile
|
Spinal Cord Diseases
|
Spinal Cord Injuries
|
Spinal Muscular Atrophy, Distal, X-Linked 3
|
Spinocerebellar Ataxias
|
Splenomegaly
|
Stomatitis
|
Stroke
|
Subarachnoid Hemorrhage
|
Drug Dependence
|
Sunburn
|
Syndactyly
|
Syndactyly, Type 3
|
Tachycardia, Ventricular
|
Telangiectasia, Hereditary Hemorrhagic
|
Testicular Microlithiasis
|
Thoracic Neoplasms
|
Thrombocytopenia
|
Thrombocytopenia, Platelet Dysfunction, Hemolysis, And Imbalanced Globin Synthesis
|
Thrombotic Microangiopathies
|
Thymoma
|
Thymus Neoplasms
|
Thyroid Diseases
|
Tongue Neoplasms
|
Transient Myeloproliferative Disorder Of Down Syndrome
|
Transposition Of Great Vessels
|
Tremor
|
Turcot Syndrome
|
Ulnar-Mammary Syndrome
|
Urinary Bladder, Overactive
|
Urinary Retention
|
Urogenital Neoplasms
|
Uterine Neoplasms
|
Vascular System Injuries
|
Ventricular Premature Complexes
|
Vestibular Diseases
|
Vulvar Lichen Sclerosus
|
Waardenburg Syndrome Type 2
|
Waardenburg Syndrome, Type 4c
|
Weight Gain
|
Nephroblastoma
|
Witkop Syndrome
|
Wittwer Syndrome
|
Xeroderma Pigmentosum, Complementation Group D
|
Aberrant Crypt Foci
|
Yemenite Deaf-Blind Hypopigmentation Syndrome
|
Abortion, Spontaneous
|
Abruptio Placentae
|
Acrocallosal Syndrome
|
Acrocapitofemoral Dysplasia
|
Acromicric Dysplasia
|
Adenocarcinoma, Clear Cell
|
Adenoma, Liver Cell
|
Adrenocortical Carcinoma, Hereditary
|
Agenesis Of Corpus Callosum
|
Alagille Syndrome
|
Alcohol Dependence
|
Androgenetic Alopecia
|
Alveolar Capillary Dysplasia
|
Ameloblastoma
|
Amphetamine-Related Disorders
|
Amyotrophic Lateral Sclerosis
|
Amyotrophic Lateral Sclerosis 2, Juvenile
|
Anauxetic Dysplasia
|
Androgen-Insensitivity Syndrome
|
Anemia
|
Anemia, Dyserythropoietic, Congenital
|
Anemia, Hemolytic
|
Ankylosis
|
Anodontia
|
Anoxia
|
Antley-Bixler Syndrome Phenotype
|
Thoracic Aortic Aneurysm
|
Aortic Rupture
|
Aortic Valve, Calcification Of
|
Arnold-Chiari Malformation
|
Arrhythmogenic Right Ventricular Dysplasia, Familial, 1
|
Arteriosclerosis
|
Arthritis, Experimental
|
Ataxia
|
Ataxia With Vitamin E Deficiency
|
Atrial Septal Defect 2
|
Auditory Neuropathy, Autosomal Dominant, 1
|
Balkan Nephropathy
|
Barakat Syndrome
|
Basal Ganglia Diseases
|
Beckwith-Wiedemann Syndrome
|
Behcet's Syndrome
|
Beta-Thalassemia
|
Beta-Ureidopropionase Deficiency
|
Birt-Hogg-Dube Syndrome
|
Bone Diseases, Metabolic
|
Bone Fragility With Contractures, Arterial Rupture, And Deafness
|
Bone Neoplasms
|
Brachydactyly
|
Brachydactyly Type A1
|
Bradycardia
|
Brain Diseases, Metabolic, Inborn
|
Brain Injuries
|
Brain Ischemia
|
Chronic Bronchitis
|
Brugada Syndrome 8
|
Bulbospinal Neuronopathy, X-Linked Recessive
|
Burns, Chemical
|
Cafe Au Lait Spots, Multiple
|
Carcinoma, Lobular
|
Carcinoma, Merkel Cell
|
Carcinoma, Squamous Cell Of Head And Neck
|
Carcinosarcoma
|
Cardioencephalomyopathy, Fatal Infantile, Due To Cytochrome C Oxidase Deficiency
|
Cardiomyopathy, Dilated, 1ee
|
Cardiomyopathy, Dilated, 1g
|
Cardiomyopathy, Dilated, 1y
|
Cardiomyopathy, Familial Hypertrophic, 1
|
Cardiomyopathy, Familial Hypertrophic, 14
|
Cardiomyopathy, Familial Hypertrophic, 3
|
Cardiomyopathy, Familial Hypertrophic, 9
|
Cardiovascular Abnormalities
|
Carotid Artery Diseases
|
Cartilage Diseases
|
Cartilage-Hair Hypoplasia
|
Cataract
|
Caudal Duplication Anomaly
|
Celiac Disease
|
Central Nervous System Neoplasms
|
Cerebellar Diseases
|
Cerebral Cavernous Malformations 2
|
Cerebrooculofacioskeletal Syndrome 2
|
Cerebrovascular Disorders
|
Charge Syndrome
|
Child Development Disorders, Pervasive
|
Sclerosing Cholangitis
|
Cholestasis, Intrahepatic
|
Chondrosarcoma, Mesenchymal
|
Choroidal Neovascularization
|
Chromosome 17 Deletion
|
Chromosome Aberrations
|
Chromosome Breakage
|
Ciliary Motility Disorders
|
Clear-Cell Metastatic Renal Cell Carcinoma
|
Clubfoot
|
Coach Syndrome
|
Coffin-Siris Syndrome
|
Cognitive Impairment
|
Complement Component 5 Deficiency
|
Complement Component 6 Deficiency
|
Copper-Overload Cirrhosis
|
Corneal Neovascularization
|
Coronary Aneurysm
|
Coronary Heart Disease
|
Coronary Vasospasm
|
Craniofacial Dysostosis
|
Craniopharyngioma
|
Critical Illness
|
Crohn's Disease
|
Cushing's Symphalangism
|
Cutis Gyrata Syndrome Of Beare And Stevenson
|
Cysts
|
Cytochrome-C Oxidase Deficiency
|
Dandy-Walker Syndrome
|
Deafness, Autosomal Dominant 28
|
Deafness, Autosomal Dominant 2a
|
Deafness, Autosomal Dominant 2b
|
Deafness, Autosomal Dominant Nonsyndromic Sensorineural 17
|
Deafness, Autosomal Recessive 1a
|
Deafness, Autosomal Recessive 35
|
Demyelinating Diseases
|
Dent Disease 1
|
Dent Disease 2
|
Unipolar Depression
|
Dermatitis, Contact
|
Diabetes Complications
|
Gestational Diabetes
|
Diabetes Mellitus, Type 1
|
Diabetic Angiopathies
|
Diabetic Retinopathy
|
Diaphragmatic Hernia 3
|
Distal Myopathies
|
Double Outlet Right Ventricle
|
Down Syndrome
|
Duane Retraction Syndrome
|
Dwarfism
|
Dyschromatosis Symmetrica Hereditaria 1
|
Dyslipidemias
|
Emphysema
|
Epilepsy
|
Erythrokeratodermia Variabilis
|
Eye Diseases
|
Familial Dilated Cardiomyopathy
|
Familial Wilms Tumor 2
|
Fanconi Anemia, Complementation Group N
|
Fatigue
|
Female Urogenital Diseases
|
Fetal Death
|
Fetal Growth Retardation
|
Fibrosis
|
Fractures, Bone
|
Gastrointestinal Stromal Tumors
|
Genital Diseases, Male
|
Glaucoma 1, Open Angle, A
|
Glaucoma, Primary Open Angle
|
Gliosarcoma
|
Gliosis
|
Glucose Intolerance
|
Goldenhar Syndrome
|
Greig Cephalopolysyndactyly Syndrome
|
Growth Disorders
|
Growth Mental Deficiency Syndrome Of Myhre
|
Hajdu-Cheney Syndrome
|
Hallermann's Syndrome
|
Hamartoma
|
Hearing Loss
|
Hearing Loss, Sensorineural
|
Heart Diseases
|
Heart Septal Defects
|
Heart Septal Defects, Atrial
|
Helicobacter Infections
|
Hemangioma, Cavernous, Central Nervous System
|
Hematologic Diseases
|
Hematuria
|
Hemochromatosis
|
Hemolysis
|
Hepatitis
|
Hepatitis, Animal
|
Hepatoblastoma
|
Hepatorenal Syndrome
|
Hereditary Myopathy With Early Respiratory Failure
|
Hereditary Spastic Paralysis, Infantile Onset Ascending
|
Hernia, Inguinal
|
Hernias, Diaphragmatic, Congenital
|
Heterotaxy Syndrome
|
Hodgkins Lymphoma
|
Holoprosencephaly 7
|
Holoprosencephaly 9
|
Hydrocephalus
|
Hyperemia
|
Hypereosinophilic Syndrome
|
Hyperinsulinism
|
Hypercholesterolemia, Familial
|
Hyperplasia
|
Hypertension, Pregnancy-Induced
|
Hypertension, Renal
|
Hypertension, Renovascular
|
Hypertriglyceridemia
|
Hypobetalipoproteinemia, Familial, Apolipoprotein B
|
Hypopigmentation
|
Hypoplastic Left Heart Syndrome
|
Hypospadias 1, X-Linked
|
Hypothalamic Hamartomas
|
Hypotrichosis And Recurrent Skin Vesicles
|
Hypotrichosis-Lymphedema-Telangiectasia Syndrome
|
Hypoxia-Ischemia, Brain
|
Immunologic Deficiency Syndromes
|
Intestinal Neoplasms
|
Intestinal Perforation
|
Iridogoniodysgenesis, Dominant Type
|
Iridogoniodysgenesis Type1
|
Jaw Abnormalities
|
Joubert Syndrome 1
|
Joubert Syndrome 7
|
Juvenile Polyposis With Hereditary Hemorrhagic Telangiectasia
|
Kabuki Syndrome
|
Keloid
|
Keratoacanthoma Familial
|
Kidney Failure, Chronic
|
Lacrimoauriculodentodigital Syndrome
|