Breast Carcinoma
|
Prostatic Neoplasms
|
Craniofacial Abnormalities
|
Stomach Neoplasms
|
Hepatocellular Carcinoma
|
Liver Cirrhosis, Experimental
|
Lung Neoplasms
|
Colorectal Cancer
|
Carcinoma, Adenoid Cystic
|
Leukemia, Myeloid, Acute
|
Adenocarcinoma
|
Urinary Bladder Neoplasms
|
Neoplasm Invasiveness
|
Colonic Neoplasm
|
Endometriosis
|
Rheumatoid Arthritis
|
Arthritis, Juvenile
|
Melanoma
|
Diabetes Mellitus, Type 2
|
Ovarian Neoplasms
|
Cell Transformation, Neoplastic
|
Pancreatic Carcinoma
|
Autism
|
Lung Adenocarcinoma
|
Neoplasm Metastasis
|
Liver Neoplasms
|
Disease Progression
|
Carcinoma
|
Myocardial Ischemia
|
Squamous Cell Carcinoma
|
Obesity
|
Intellectual Disability
|
Drug-Induced Liver Injury
|
Acute Lymphoblastic Leukemia
|
Mammary Neoplasms, Experimental
|
Neoplasms
|
Autism Spectrum Disorder
|
Diabetes Mellitus, Experimental
|
Esophageal Squamous Cell Carcinoma
|
Skin Neoplasms
|
Glioblastoma Multiforme
|
Renal Cell Carcinoma
|
Medulloblastoma
|
Glioma
|
Arsenic Poisoning
|
Carcinoma, Non-Small-Cell Lung
|
Mammary Neoplasms, Animal
|
Endometrial Neoplasm
|
Hypertension
|
Small Cell Lung Carcinoma
|
Skin Diseases
|
Insulin Resistance
|
Brain Ischemia
|
Heart Defects, Congenital
|
Osteosarcoma
|
Polycystic Ovary Syndrome
|
Inflammation
|
Psoriasis
|
Esophageal Neoplasms
|
Kidney Disease
|
Mesothelioma, Malignant
|
Sezary Syndrome
|
Fatty Liver
|
Peripheral Neuropathy
|
Leukemia, Promyelocytic, Acute
|
Neuroblastoma
|
Nerve Degeneration
|
Drug Dependence
|
Necrosis
|
Amyotrophic Lateral Sclerosis 1
|
Systemic Lupus Erythematosus
|
Infertility, Female
|
Lymphoma, T-Cell, Cutaneous
|
Lymphoma, T-Cell
|
Myocardial Infarction
|
Ulcerative Colitis
|
Precancerous Conditions
|
Crohn's Disease
|
Micronuclei, Chromosome-Defective
|
Hernia, Diaphragmatic
|
Neoplasm Recurrence, Local
|
Neoplasms, Experimental
|
Carcinoma, Transitional Cell
|
Cocaine Dependence
|
Lung Diseases
|
Male Infertility
|
Reperfusion Injury
|
Leukemia
|
Uterine Cervical Neoplasms
|
Mouth Neoplasms
|
Brain Injuries
|
Disease Models, Animal
|
Hiv Infections
|
Chronic Lymphocytic Leukemia
|
Mesothelioma
|
Kidney Failure, Chronic
|
Schizophrenia
|
Nervous System Diseases
|
Thyroid Carcinoma
|
Female Urogenital Diseases
|
Basal Cell Carcinoma
|
Limb Deformities, Congenital
|
Osteoarthritis
|
Salivary Gland Neoplasm
|
Chromosome Aberrations
|
Liver Neoplasms, Experimental
|
Heart Diseases
|
Precursor B-Cell Lymphoblastic Leukemia-Lymphoma
|
Leukemia-Lymphoma, Adult T-Cell
|
Seizures
|
Heart Failure
|
Carcinoma, Squamous Cell Of Head And Neck
|
Diabetes Mellitus, Type 1
|
Hyperplasia
|
Adrenocortical Carcinoma
|
Androgenetic Alopecia
|
Cholestasis
|
Liver Cirrhosis
|
Brain Neoplasms
|
Astrocytoma
|
Drug-Related Side Effects And Adverse Reactions
|
Toxic Epidermal Necrolysis
|
Influenza, Human
|
Cardiac Hypertrophy
|
Heat Stroke
|
Tetralogy Of Fallot
|
Cardiomyopathies
|
Alzheimer's Disease
|
Cholangiocarcinoma
|
Myelodysplastic Syndromes
|
Head And Neck Neoplasms
|
Neural Tube Defects
|
Non-Alcoholic Fatty Liver Disease
|
Recurrence
|
Burkitt Lymphoma
|
Adenocarcinoma Of Esophagus
|
Neoplasms, Germ Cell And Embryonal
|
Growth Disorders
|
Asthma
|
Nasopharyngeal Carcinoma
|
Genetic Predisposition To Disease
|
Atherosclerosis
|
Arthritis, Experimental
|
Microcephaly
|
Skin Abnormalities
|
Leukemia, Myelomonocytic, Juvenile
|
Chronic Myelogenous Leukemia
|
Bone Diseases, Developmental
|
Prostatic Intraepithelial Neoplasia
|
Precursor T-Cell Lymphoblastic Leukemia-Lymphoma
|
Epilepsy
|
Abnormalities, Multiple
|
Hemangiosarcoma
|
Leukemia, Myeloid
|
Metabolic Syndrome X
|
Carcinoma, Pancreatic Ductal
|
Dilated Cardiomyopathy
|
Leukemia, Lymphoid
|
Spinocerebellar Ataxias
|
Status Epilepticus
|
Tooth Abnormalities
|
Anxiety Disorder
|
Cognitive Impairment
|
Ischemia
|
Coffin-Siris Syndrome
|
Fibrosis
|
Infarction, Middle Cerebral Artery
|
Dermatitis, Allergic Contact
|
Lymphoma, Follicular
|
Nervous System Malformations
|
Multiple Myeloma
|
Amphetamine-Related Disorders
|
Weight Gain
|
Mental Retardation, X-Linked
|
Glomerulonephritis
|
Lymphoma, Large B-Cell, Diffuse
|
Atrial Fibrillation
|
Hand Deformities, Congenital
|
Craniosynostoses
|
Carcinogenesis
|
Deafness
|
Acute Kidney Injury
|
Myocardial Reperfusion Injury
|
Hernias, Diaphragmatic, Congenital
|
Dermatitis, Contact
|
Hyperalgesia
|
Hyperglycemia
|
Diabetes Mellitus
|
Osteoporosis
|
Pulmonary Hypertension
|
Diabetic Nephropathy
|
Anoxia
|
Pilomatrixoma
|
Dyslipidemias
|
Poisoning
|
Prenatal Exposure Delayed Effects
|
Proteinuria
|
Pulmonary Fibrosis
|
Radiation Injuries, Experimental
|
Enterocolitis, Necrotizing
|
Cone-Rod Dystrophy 2
|
Rhabdomyosarcoma, Alveolar
|
Sarcoma
|
Brain Diseases
|
Lipidoses
|
Fanconi Anemia
|
Sjogren Syndrome
|
Primary Biliary Cirrhosis
|
Chromosome Breakage
|
Lymphatic Metastasis
|
Cleft Lip
|
Lymphoma
|
Meier-Gorlin Syndrome
|
Memory Disorders
|
Nephroblastoma
|
Coronary Artery Disease
|
Adrenal Gland Neoplasms
|
Liver Diseases, Parasitic
|
Neurodegenerative Diseases
|
Leukemia, Megakaryoblastic, Of Down Syndrome
|
Kidney Neoplasms
|
Diabetic Angiopathies
|
Nerve Sheath Neoplasms
|
Ovarian Cysts
|
Sciatic Neuropathy
|
Microsatellite Instability
|
Bipolar Disorder
|
Parkinsonian Disorders
|
Carcinoma, Ductal, Breast
|
Splenomegaly
|
Language Development Disorders
|
Parkinson's Disease
|
Dementia
|
Adenomatous Polyposis Coli
|
Polycystic Kidney, Autosomal Dominant
|
Respiratory Distress Syndrome, Adult
|
Turcot Syndrome
|
Cholestasis, Intrahepatic
|
Hyperlipidemias
|
Acute Lung Injury
|
Colorectal Neoplasms, Hereditary Nonpolyposis
|
Chloracne
|
Amyotrophic Lateral Sclerosis
|
Hepatomegaly
|
Pituitary Hormone Deficiency, Combined, 2
|
Substance Withdrawal Syndrome
|
Urologic Neoplasms
|
Hepatitis, Chronic
|
Musculoskeletal Abnormalities
|
Cardiomyopathy, Hypertrophic
|
Hypoglycemia
|
Leukemia, T-Cell
|
Psoriatic Arthritis
|
Congenital Abnormalities
|
Learning Disorders
|
Ventricular Dysfunction, Left
|
Fever
|
Microphthalmos
|
Metabolic Diseases
|
Meningioma
|
Muscular Diseases
|
Copper-Overload Cirrhosis
|
Idiopathic Pulmonary Fibrosis
|
Autoimmune Disease
|
Barrett's Esophagus
|
Anodontia
|
Alcoholic Liver Cirrhosis
|
Multiple Sclerosis
|
Primary Ovarian Insufficiency
|
Bare Lymphocyte Syndrome 2
|
Testicular Neoplasms
|
Huntington Disease
|
Abortion, Spontaneous
|
Bowen's Disease
|
Hypertrophy
|
Thrombocytopenia
|
Lymphoma, T-Cell, Peripheral
|
Atopic Eczema
|
Aging, Premature
|
Breast Neoplasms, Male
|
Ceroid Lipofuscinosis, Neuronal 1, Infantile
|
Thymoma
|
Sleep Disorders, Circadian Rhythm
|
Hearing Loss
|
Celiac Disease
|
Cataract
|
Intestinal Neoplasms
|
Liver Diseases
|
Neuroectodermal Tumors, Primitive
|
Lymphoma, Non-Hodgkin
|
Testicular Germ Cell Tumor
|
Neurotoxicity Syndromes
|
Neurologic Manifestations
|
Neuroendocrine Tumors
|
Thyroid Cancer, Follicular
|
Thyroid Cancer, Papillary
|
Clubfoot
|
Thyroid Diseases
|
Dermatitis
|
Mandibulofacial Dysostosis
|
Cyclopia
|
Hodgkins Lymphoma
|
Nephrotic Syndrome
|
Asbestosis
|
Tongue Neoplasms
|
Nephrosis
|
Unipolar Depression
|
Gallbladder Neoplasm
|
Neoplasms, Squamous Cell
|
Neoplasms, Second Primary
|
Gastrointestinal Diseases
|
Gastrointestinal Neoplasms
|
Trigeminal Neuralgia
|
Atrophy
|
Myotonic Dystrophy
|
Myopia
|
Hereditary Breast And Ovarian Cancer Syndrome
|
Uremia
|
Creutzfeldt Jacob Disease
|
Hepatoblastoma
|
Urogenital Neoplasms
|
Uterine Neoplasms
|
Uveitis
|
Combined Cellular And Humoral Immune Defects With Granulomas
|
Vascular Diseases
|
Congenital Central Hypoventilation Syndrome
|
Ventricular Remodeling
|
Hepatitis
|
Vulvar Lichen Sclerosus
|
Carcinoma, Intraductal, Noninfiltrating
|
Waardenburg Syndrome Type 2
|
Iga Glomerulonephritis
|
Adenoma
|
Jaw Abnormalities
|
Edema
|
Emphysema
|
Encephalomyelitis, Autoimmune, Experimental
|
Body Weight
|
Bone Diseases, Metabolic
|
Aicardi-Goutieres Syndrome
|
Keloid
|
Keratoconus
|
Premature Birth
|
Acrocallosal Syndrome
|
Adenoma, Liver Cell
|
Keratosis
|
Birth Weight
|
Cerebrooculofacioskeletal Syndrome 1
|
Psychoses, Substance-Induced
|
Psychomotor Disorders
|
Chronic Obstructive Pulmonary Disease
|
Kidney Tubular Necrosis, Acute
|
Acute Coronary Syndrome
|
Weight Loss
|
Carcinoma, Ductal
|
Polyploidy
|
Polydactyly
|
Respiratory Insufficiency
|
Leber Congenital Amaurosis
|
Pneumonia
|
Reticuloendotheliosis, Familial, With Eosinophilia
|
Retinal Degeneration
|
Uterine Fibroid
|
Immunoblastic Lymphadenopathy
|
Williams Syndrome
|
Rett Syndrome
|
Leukemia, Monocytic, Acute
|
Dwarfism
|
Phyllodes Tumor
|
Cecal Neoplasms
|
Chondrosarcoma, Extraskeletal Myxoid
|
Leukemia, Myelomonocytic, Acute
|
Rubinstein-Taybi Syndrome
|
Peters Anomaly
|
Peritoneal Neoplasms
|
Hypotension
|
Corneal Dystrophy, Posterior Polymorphous, 1
|
Ewing Sarcoma
|
Sarcoma Family Syndrome Of Li And Fraumeni
|
Brachydactyly
|
Anemia
|
Down Syndrome
|
Eye Abnormalities
|
Systemic Scleroderma
|
Alcohol Dependence
|
Seckel Syndrome 1
|
Glucose Intolerance
|
Sepsis
|
Azoospermia
|
Severe Combined Immunodeficiency, Autosomal Recessive, T Cell-Negative, B Cell-Negative, Nk Cell-Positive
|
Lipodystrophy
|
Parietal Foramina
|
Familial Primary Pulmonary Hypertension
|
Liposarcoma, Myxoid
|
Anophthalmos
|
Xeroderma Pigmentosum
|
Left Ventricular Hypertrophy
|
Papilloma
|
Pancreatitis
|
Pancreatic Agenesis, Congenital
|
Pain
|
Graves Disease
|
Lead Poisoning
|
Diabetes Mellitus, Transient Neonatal, 1
|
Ophthalmoplegia, Chronic Progressive External
|
Splenic Diseases
|
Oligospermia
|
Branchio-Oto-Renal Syndrome
|
Lung Diseases, Obstructive
|
Lung Injury
|
Oligodendroglioma
|
Cardiovascular Abnormalities
|
Ocular Hypertension
|
Stroke
|
Occupational Diseases
|
Chronobiology Disorders
|
Mitochondrial Diseases
|
Migraine Disorder
|
Nystagmus, Congenital
|
Gestational Diabetes
|
Lymphoma, Large-Cell, Anaplastic
|
Mental Retardation-Hypotonic Facies Syndrome, X-Linked, 1
|
Mental Retardation, X-Linked 45
|
Mental Retardation, X-Linked, Syndromic 10
|
Mental Retardation, X-Linked 79
|
Mental Retardation, X-Linked, Syndromic, Jarid1c-Related
|
Mental Retardation, X-Linked, Syndromic, Turner Type
|
Mental Retardation, X-Linked, With Or Without Seizures, Arx-Related
|
Mental Retardation, X-Linked, With Panhypopituitarism
|
Mercury Poisoning, Nervous System
|
Methylmalonic Acidemia
|
Microcephalic Osteodysplastic Primordial Dwarfism, Type Ii
|
Microphthalmia, Isolated 2
|
Microphthalmia, Isolated 3
|
Microphthalmia, Isolated, With Cataract 2
|
Microphthalmia, Isolated, With Coloboma 3
|
Microphthalmia, Syndromic 3
|
Microphthalmia, Syndromic 5
|
Microtia, Hearing Impairment, And Cleft Palate
|
Migraine Without Aura
|
Mild Cognitive Impairment
|
Mody, Type 6
|
Morphine Dependence
|
Motor Skills Disorders
|
Mouth Diseases
|
Movement Disorder
|
Mowat-Wilson Syndrome
|
Muir-Torre Syndrome
|
Multiple Chemical Sensitivity
|
Multiple Endocrine Neoplasia Type 1
|
Multiple Organ Failure
|
Muscle Hypotonia
|
Muscular Atrophy
|
Muscular Dystrophies, Limb-Girdle
|
Muscular Dystrophy, Animal
|
Cardiomyopathy, Dilated, 3b
|
Musculoskeletal Pain
|
Mycobacterium Infections
|
Mycobacterium Infections, Nontuberculous
|
Myelodysplastic-Myeloproliferative Diseases
|
Myeloproliferative Disorder, Chronic, With Eosinophilia
|
Myeloproliferative Syndrome, Transient
|
Myoclonic Epilepsy, Juvenile
|
Myoclonus
|
Nail-Patella Syndrome
|
Nasopharyngeal Neoplasm
|
Neointima
|
Neoplasms, Radiation-Induced
|
Neoplastic Processes
|
Nephritis
|
Nephritis, Interstitial
|
Nephronophthisis 7
|
Neuropathic Pain
|
Neurilemmoma
|
Neurodevelopmental Disorders
|
Neuroectodermal Tumors
|
Neurofibromatosis 1
|
Neurogenic Inflammation
|
Neuromuscular Manifestations
|
Neuropathy, Painful
|
Neutropenia, Nonimmune Chronic Idiopathic, Adult
|
Neutropenia, Severe Congenital, Autosomal Dominant 1
|
Neutropenia, Severe Congenital, Autosomal Dominant 2
|
Nicolaides Baraitser Syndrome
|
Night Blindness
|
Nijmegen Breakage Syndrome-Like Disorder
|
Noonan Syndrome
|
Noonan Syndrome 4
|
No-Reflow Phenomenon
|
Obsessive-Compulsive Disorder
|
Oculoauricular Syndrome
|
Oculodigitoesophagoduodenal Syndrome
|
Oculootoradial Syndrome
|
O'Donnell Pappas Syndrome
|
Optic Nerve Diseases
|
Optic Nerve Hypoplasia, Bilateral
|
Oral Submucous Fibrosis
|
Orofacial Cleft 5
|
Ossification, Heterotopic
|
Osteitis Deformans
|
Ovarian Epithelial Cancer
|
Pain Insensitivity, Congenital
|
Pallister-Hall Syndrome
|
Pancreatic Cancer, Adult
|
Pancreatic Diseases
|
Panhypopituitarism X-Linked
|
Papilloma, Choroid Plexus
|
Papillorenal Syndrome
|
Paralysis
|
Paraquat Lung
|
Parietal Foramina 2
|
Parietal Foramina With Cleidocranial Dysplasia
|
Partington X-Linked Mental Retardation Syndrome
|
Peanut Hypersensitivity
|
Pelger-Huet Anomaly
|
Cousin Syndrome
|
Penile Diseases
|
Penile Neoplasms
|
Peripheral Demyelinating Neuropathy, Central Dysmyelination, Waardenburg Syndrome, And Hirschsprung Disease
|
Pheochromocytoma
|
Photophobia
|
Pick Disease Of The Brain
|
Piebaldism
|
Pierre Robin Syndrome
|
Pigmentation Disorders
|
Pitt-Hopkins Syndrome
|
Pituitary Acth Hypersecretion
|
Pituitary Hormone Deficiency, Combined, 1
|
Pituitary Hormone Deficiency, Combined, 4
|
Plaque, Amyloid
|
Plaque, Atherosclerotic
|
Platelet Disorder, Familial, With Associated Myeloid Malignancy
|
Pleuropulmonary Blastoma
|
Pneumoconiosis
|
Pneumonia, Pneumococcal
|
Polydactyly, Postaxial
|
Polydactyly, Preaxial 4
|
Polyendocrinopathies, Autoimmune
|
Polyps
|
Popliteal Pterygium Syndrome
|
Prader-Willi Syndrome
|
Preaxial Deficiency, Postaxial Polydactyly And Hypospadias
|
Preeclampsia
|
Premature Ovarian Failure 3
|
Premature Ovarian Failure 5
|
Premature Ovarian Failure 6
|
Premature Ovarian Failure 7
|
Prenatal Injuries
|
Primary Myelofibrosis
|
Primrose Syndrome
|
Progeria
|
Progressive External Ophthalmoplegia With Mitochondrial Dna Deletions, Autosomal Dominant, 1
|
Progressive External Ophthalmoplegia With Mitochondrial Dna Deletions, Autosomal Dominant, 4
|
Progressive External Ophthalmoplegia With Mitochondrial Dna Deletions, Autosomal Recessive
|
Progressive Hearing Loss Stapes Fixation
|
Progressive Supranuclear Palsy Atypical
|
Prolactinoma
|
Propping Zerres Syndrome
|
Prostate Cancer, Familial
|
Prostate Cancer, Hereditary, 11
|
Prostatic Neoplasms, Castration-Resistant
|
Proud Syndrome
|
Pseudohypoaldosteronism
|
Psychomotor Agitation
|
Psychosis
|
Leigh Necrotizing Encephalopathy Due To Pyruvate Carboxylase Deficiency
|
Radiation Injuries
|
Radioulnar Synostosis With Amegakaryocytic Thrombocytopenia
|
Rapp-Hodgkin Syndrome
|
Renal Cysts And Diabetes Syndrome
|
Chronic Kidney Disease
|
Renpenning Syndrome 1
|
Respiratory Tract Diseases
|
Restless Legs Syndrome
|
Reticulocytosis
|
Retinal Detachment
|
Retinal Diseases
|
Retinal Telangiectasis
|
Retinitis Pigmentosa 10
|
Retinitis Pigmentosa 31
|
Retinitis Pigmentosa 37
|
Retinoblastoma
|
Retrognathia
|
Rhabdoid Tumor
|
Rhabdoid Tumor Predisposition Syndrome 1
|
Rhabdomyosarcoma
|
Rhabdomyosarcoma, Embryonal
|
Allergic Rhinitis
|
Rhinitis, Allergic, Perennial
|
Rickets
|
Ring Dermoid Of Cornea
|
Saethre-Chotzen Syndrome With Eyelid Anomalies
|
Salivary Gland Adenoma, Pleomorphic
|
Sarcoidosis
|
Sarcopenia
|
Schinzel-Giedion Syndrome
|
Schwannomatosis
|
Scrapie
|
Sebaceous Gland Neoplasms
|
Seckel Syndrome 2
|
Sensory Ataxic Neuropathy, Dysarthria, And Ophthalmoparesis
|
Serum Sickness
|
Severe Combined Immunodeficiency With Microcephaly, Growth Retardation, And Sensitivity To Ionizing Radiation
|
Shock, Cardiogenic
|
Short Stature, Idiopathic, Autosomal
|
Short Stature, Idiopathic, X-Linked
|
Silicosis
|
Silver-Russell Syndrome
|
Sinonasal Undifferentiated Carcinoma
|
Skeletal Defects, Genital Hypoplasia, And Mental Retardation
|
Insomnia
|
Solitary Fibrous Tumors
|
Spastic Paraplegia, Hereditary
|
Specific Granule Deficiency
|
Spinal Cord Diseases
|
Spinal Cord Injuries
|
Spinal Dysraphism
|
Spinal Muscular Atrophy With Respiratory Distress 1
|
Spinocerebellar Ataxia 17
|
Spinocerebellar Ataxia, Autosomal Recessive 1
|
Spinocerebellar Ataxia, Autosomal Recessive 5
|
Split-Hand-Foot Malformation 4
|
Spondylarthritis
|
Ankylosing Spondylitis
|
Spondylo-Megaepiphyseal-Metaphyseal Dysplasia
|
Stereotypic Movement Disorder
|
Stomatognathic System Abnormalities
|
Sunburn
|
Progressive Supranuclear Palsy
|
Supratentorial Neoplasms
|
Sveinsson Chorioretinal Atrophy
|
Sweat Gland Neoplasms
|
Syndactyly, Type V
|
Synpolydactyly 1
|
Systemic Vasculitis
|
Tachycardia
|
Tauopathies
|
T-Cell Immunodeficiency, Congenital Alopecia And Nail Dystrophy
|
Teratogenesis
|
Thoracic Diseases
|
Thoracic Neoplasms
|
Thrombocytopenia, Platelet Dysfunction, Hemolysis, And Imbalanced Globin Synthesis
|
Thrombosis
|
Thymic Epithelial Tumor
|
Thymus Neoplasms
|
Thyroid Carcinoma, Anaplastic
|
Thyroid Hormone Resistance, Generalized, Autosomal Dominant
|
Thyroid Hormone Resistance, Generalized, Autosomal Recessive
|
Thyroid Hormone Resistance, Selective Pituitary
|
Thyroid Hormone Resistance Syndrome
|
Thyroiditis, Autoimmune
|
Tietz Syndrome
|
T-Lymphocytopenia
|
Nicotine Dependence
|
Tooth Agenesis, Selective, 3
|
Townes-Brocks Syndrome
|
Transient Myeloproliferative Disorder Of Down Syndrome
|
Translocation, Genetic
|
Trichorhinophalangeal Syndrome, Type I
|
Trichorhinophalangeal Syndrome, Type Iii
|
Trichotillomania
|
Trisomy
|
Turner Syndrome
|
Ulcer
|
Ulnar-Mammary Syndrome
|
Upper Extremity Deformities, Congenital
|
Ureteral Neoplasms
|
Urinary Bladder Calculi
|
Urticaria
|
Van Der Woude Syndrome
|
Vascular System Injuries
|
Vater Association
|
Vertical Talus, Congenital
|
Vipoma
|
Vitamin A Deficiency
|
Vitamin D Deficiency
|
Rickets, Hereditary Vitamin D-Resistant
|
Waardenburg Syndrome
|
Waardenburg Syndrome Type 2a
|
Waardenburg Syndrome, Type 2d
|
Waardenburg Syndrome, Type 4c
|
Wagr Syndrome
|
Werner Syndrome
|
Winkelman Bethge Pfeiffer Syndrome
|
Witkop Syndrome
|
Wittwer Syndrome
|
Wounds And Injuries
|
Xeroderma Pigmentosum, Complementation Group B
|
Xeroderma Pigmentosum, Complementation Group C
|
Xeroderma Pigmentosum, Complementation Group D
|
Xeroderma Pigmentosum, Complementation Group E
|
Xeroderma Pigmentosum, Complementation Group F
|
Xeroderma Pigmentosum, Complementation Group G
|
Xeroderma Pigmentosum, Variant Type
|
Xfe Progeroid Syndrome
|
Yellow Nail Syndrome
|
46, Xx Disorders Of Sex Development
|
Yemenite Deaf-Blind Hypopigmentation Syndrome
|
46, Xy Disorders Of Sex Development
|
46, Xy Sex Reversal 5
|
Abdominal Obesity Metabolic Syndrome
|
Aberrant Crypt Foci
|
Abortion, Habitual
|
Acrocephalosyndactylia
|
Acromicric Dysplasia
|
Acth Deficiency, Isolated
|
Acute-Phase Reaction
|
Adenocarcinoma, Clear Cell
|
Adenocarcinoma, Follicular
|
Adenocarcinoma, Mucinous
|
Adrenal Insufficiency
|
Adrenocortical Carcinoma, Hereditary
|
Adrenoleukodystrophy
|
Agenesis Of Corpus Callosum
|
Albinism Ocular Late Onset Sensorineural Deafness
|
Albinism, Oculocutaneous
|
Albuminuria
|
Alopecia Areata
|
Alopecia Universalis
|
Alpha-Beta T-Cell Lymphopenia With Gamma-Delta T-Cell Expansion, Severe Cytomegalovirus Infection, And Autoimmunity
|
Alpha-Thalassemia Myelodysplasia Syndrome
|
Alveolar Capillary Dysplasia
|
Alveolitis, Extrinsic Allergic
|
Amelogenesis Imperfecta, Type Iv
|
Amino Acid Metabolism, Inborn Errors
|
Amnesia
|
Amyloidosis
|
Amyotrophic Lateral Sclerosis 10
|
Amyotrophic Lateral Sclerosis 4, Juvenile
|
Amyotrophic Lateral Sclerosis 6, Autosomal Recessive
|
Amyotrophic Lateral Sclerosis 9
|
Anaplasia
|
Androgen-Insensitivity Syndrome
|
Anemia, Aplastic
|
Anemia, Dyserythropoietic, Congenital
|
Anemia, Hypochromic Microcytic
|
Anemia, Sideroblastic
|
Aneuploidy
|
Aneurysm, Dissecting
|
Angelman Syndrome
|
Angioedema
|
Aniridia
|
Aniridia Cerebellar Ataxia Mental Deficiency
|
Aniridia, Type 2
|
Anonychia Congenita
|
Anovulation
|
Anuria
|
Aortic Aneurysm
|
Aortic Diseases
|
Aphakia, Congenital Primary
|
Apraxias
|
Arnold-Chiari Malformation
|
Cardiac Arrhythmia
|
Carotid Artery Diseases
|
Carotid Intimal Medial Thickness 1
|
Arterial Occlusive Diseases
|
Arthritis
|
Arthrogryposis
|
Asphyxia Neonatorum
|
Aspirin Induced Asthma
|
Asthma, Nasal Polyps, And Aspirin Intolerance
|
Ataxia
|
Ataxia Telangiectasia
|
Athabaskan Brainstem Dysgenesis
|
Atrial Septal Defect 2
|
Atrial Septal Defect 4
|
Atrichia With Papular Lesions
|
Atr-X Syndrome
|
Auditory Perceptual Disorders
|
Autoimmune Polyendocrinopathy Syndrome, Type 1
|
Balkan Nephropathy
|
Bamforth Syndrome
|
Barakat Syndrome
|
Basal Cell Nevus Syndrome
|
Behcet's Syndrome
|
Biliary Tract Neoplasms
|
Blepharophimosis, Ptosis, And Epicanthus Inversus
|
Blepharophimosis Syndrome Type 1
|
Bloom Syndrome
|
Bohring Syndrome
|
Bone Resorption
|
Borjeson-Forssman-Lehmann Syndrome
|
Bpes With Duane Retraction Syndrome
|
Brachydactyly-Syndactyly Syndrome
|
Brachydactyly, Type D
|
Brain Stem Neoplasms
|
Branchiootic Syndrome 3
|
Breast Diseases
|
Brittle Cornea Syndrome 1
|
Brugada Syndrome
|
Bulbospinal Neuronopathy, X-Linked Recessive
|
Buschke-Ollendorff Syndrome
|
Cachexia
|
Cafe-Au-Lait Spots
|
Cafe Au Lait Spots, Multiple
|
Calcinosis
|
Campomelic Dysplasia
|
Candidiasis
|
Candidiasis, Chronic Mucocutaneous
|
Candidiasis, Oral
|
Candidiasis, Vulvovaginal
|
Carbon Tetrachloride Poisoning
|
Carcinoma, Lobular
|
Carcinoma, Merkel Cell
|
Carcinoma, Small Cell
|
Cardiomyopathy, Dilated, 1t
|
Cardiotoxicity
|
Cardiovascular Disease
|
Cartilage Diseases
|
Cataract And Cardiomyopathy
|
Cataract, Autosomal Dominant
|
Cataract, Posterior Polar, 4
|
Cataract, Pulverulent, Juvenile-Onset
|
Cataract, Zonular
|
Cayler Cardiofacial Syndrome
|
Central Nervous System Diseases
|
Central Nervous System Neoplasms
|
Cerebellar Diseases
|
Cerebral Amyloid Angiopathy
|
Cerebral Amyloid Angiopathy, App-Related
|
Cerebral Hemorrhage With Amyloidosis, Hereditary, Dutch Type
|
Cerebrooculofacioskeletal Syndrome 2
|
Cerebrooculofacioskeletal Syndrome 4
|
Ceroid Lipofuscinosis, Neuronal, 6
|
Cervical Intraepithelial Neoplasia
|
Charcot-Marie-Tooth Disease
|
Charcot-Marie-Tooth Disease, Type 1d
|
Charcot-Marie-Tooth Disease, Type 4e
|
Charge Syndrome
|
Char Syndrome
|
Child Development Disorders, Pervasive
|
Cholangitis
|
Sclerosing Cholangitis
|
Chondrosarcoma, Mesenchymal
|
Chordoma
|
Chorea
|
Choreoathetosis, Hypothyroidism, And Neonatal Respiratory Distress
|
Chromosomal Instability
|
Chromosome 17 Deletion
|
Chromosome 2q37 Deletion Syndrome
|
Chromosome 5q Deletion Syndrome
|
Chromosome Deletion
|
Chromosome Disorders
|
Classical Lissencephalies And Subcortical Band Heterotopias
|
Cleft Palate
|
Cleft Palate X-Linked
|
Cleidocranial Dysplasia
|
Cockayne Syndrome
|
Colitis
|
Coloboma
|
Coloboma Of Optic Nerve
|
Colorectal Adenomatous Polyposis, Autosomal Recessive
|
Color Vision Defects
|
Corneal Diseases
|
Corneal Dystrophies, Hereditary
|
Corneal Dystrophy, Fuchs Endothelial, 6
|
Corneal Dystrophy, Posterior Polymorphous, 3
|
Coronary Artery Disease, Autosomal Dominant, 1
|
Coronary Heart Disease
|
Craniofacial Deafness Hand Syndrome
|
Craniopharyngioma
|
Craniosynostosis, Type 2
|
Cri-Du-Chat Syndrome
|
Critical Illness
|
Cryptorchidism
|
Currarino Triad
|
Cystitis
|
Cytomegalovirus Infection
|
Dandy-Walker Syndrome
|
Deafness, Autosomal Dominant 15
|
Deafness, Autosomal Dominant 23
|
Deafness, Autosomal Dominant 28
|
Deafness, Autosomal Recessive 35
|
Deafness, Autosomal Recessive 67
|
Delayed Emergence From Anesthesia
|
Demyelinating Diseases
|
Denys-Drash Syndrome
|
Major Depression
|
De Sanctis-Cacchione Syndrome
|
Developmental Disabilities
|
Dextrocardia
|
Diabetes Complications
|
Diabetes Mellitus, Insulin-Dependent, 19
|
Diabetes Mellitus, Insulin-Dependent, 20
|
Diabetes Mellitus, Neonatal, With Congenital Hypothyroidism
|
Diabetes Mellitus, Permanent Neonatal, With Cerebellar Agenesis
|
Diaphragmatic Hernia 3
|
Diarrhea
|
Diarrhea 4, Malabsorptive, Congenital
|
Diffuse Cerebral Sclerosis Of Schilder
|
Digeorge Syndrome
|
Disruptive, Impulse Control, And Conduct Disorders
|
Dosage-Sensitive Sex Reversal
|
Duane Retraction Syndrome
|
Ductus Arteriosus, Patent
|
Dwarfism, Pituitary
|
Dyschromatosis Symmetrica Hereditaria 1
|
Dysgnathia Complex
|
Dyskeratosis Congenita
|
Dyskeratosis Congenita, Autosomal Dominant
|
Dyskinesia, Drug-Induced
|
Limb Dystonia
|
Dystonia 3, Torsion, X-Linked
|
Dystonia 6, Torsion
|
Dystonic Disorders
|
Early-Onset Ataxia With Oculomotor Apraxia And Hypoalbuminemia
|
Echinococcosis
|
Ectopia Pupillae
|
Ectrodactyly-Cleft Lip-Palate Syndrome
|
Ectrodactyly, Ectodermal Dysplasia, And Cleft Lip-Palate Syndrome 3
|
Empty Sella Syndrome
|
Encephalopathy, Neonatal Severe, Due To Mecp2 Mutations
|
Endometrial Hyperplasia
|
Endotoxemia
|
Enhanced S-Cone Syndrome
|
Ependymoma
|
Epilepsy, Absence
|
Epilepsy, Generalized
|
Epilepsy, Temporal Lobe
|
Epileptic Encephalopathy, Early Infantile, 1
|
Erythrocytosis, Familial, 4
|
Esophageal Stenosis
|
Esophagitis
|
Extravasation Of Diagnostic And Therapeutic Materials
|
Facial Asymmetry
|
Facial Palsy, Congenital, Unilateral Or Bilateral
|
Facies
|
Familial Schizencephaly
|
Fanconi Anemia, Complementation Group D1
|
Fanconi Anemia, Complementation Group I
|
Fanconi Anemia, Complementation Group J
|
Fanconi Anemia, Complementation Group N
|
Farber Lipogranulomatosis
|
Fatty Liver, Alcoholic
|
Feminization
|
Fetal Death
|
Fetal Growth Retardation
|
Fibroadenoma
|
Fibrosis Of Extraocular Muscles, Congenital, 2
|
Fibrous Dysplasia Of Bone
|
Foot Deformities, Congenital
|
Fractures, Bone
|
Fragile X Syndrome
|
Frasier Syndrome
|
Frontotemporal Dementia
|
Frontotemporal Lobar Degeneration
|
Gait Disorders, Neurologic
|
Gastric Antral Vascular Ectasia
|
Gastrinoma
|
Gastrointestinal Hemorrhage
|
Genetic Diseases, Inborn
|
Genital Diseases, Male
|
Genomic Instability
|
Glaucoma
|
Glaucoma 1, Open Angle, A
|
Glaucoma, Angle-Closure
|
Glaucoma, Primary Open Angle
|
Gliosis
|
Glomerulonephritis, Membranoproliferative
|
Membranous Glomerulonephritis
|
Focal Segmental Glomerulosclerosis
|
Glucagonoma
|
Gonadal Dysgenesis, 46,Xx
|
Gonadal Dysgenesis, 46,Xy
|
Granuloma, Respiratory Tract
|
Greig Cephalopolysyndactyly Syndrome
|
Growth Mental Deficiency Syndrome Of Myhre
|
Hairy Ears, Y-Linked
|
Hand Foot Uterus Syndrome
|
Hay-Wells Syndrome
|
Noise-Induced Hearing Loss
|
Hearing Loss, Sensorineural
|
Heart Septal Defects, Atrial
|
Hemangioblastoma
|
Hematologic Diseases
|
Hematologic Neoplasms
|
Hematuria
|
Hemolytic-Uremic Syndrome
|
Hemorrhage
|
Hepatic Adenomas, Familial
|
Hepatic Encephalopathy
|
Hepatic Venoocclusive Disease With Immunodeficiency
|
Hepatitis C
|
Hereditary Autoinflammatory Diseases
|
Hereditary Sensory And Autonomic Neuropathies
|
Hereditary Sensory And Motor Neuropathy
|
Heroin Dependence
|
Heterotaxy, Visceral, 5, Autosomal
|
Hirschsprung Disease
|
Histiocytoma, Angiomatoid Fibrous
|
Hiv Seropositivity
|
Holoprosencephaly 2
|
Holoprosencephaly 4
|
Holoprosencephaly 5
|
Holoprosencephaly 9
|
Holt-Oram Syndrome
|
Hoyeraal Hreidarsson Syndrome
|
Hydrocephalus
|
Hydronephrosis
|
Hypercholesterolemia
|
Hyper-Ige Recurrent Infection Syndrome, Autosomal Dominant
|
Hyperinsulinism
|
Hyperkeratosis, Epidermolytic
|
Hyperkinesis
|
Hyperlipidemia, Combined, 2
|
Hyperlipoproteinemias
|
Hyperoxaluria
|
Hyperoxia
|
Hyperparathyroidism 1
|
Allergy
|
Hypersensitivity, Delayed
|
Hypertension, Early-Onset, Autosomal Dominant, With Severe Exacerbation In Pregnancy
|
Hyperthyroidism
|
Hyperthyroxinemia, Familial Dysalbuminemic
|
Hypertriglyceridemia
|
Hyperventilation
|
Hypoalbuminemia
|
Hypogonadism
|
Hypokalemia
|
Hypophosphatemia
|
Hypopigmentation
|
Hypopituitarism And Septooptic 'Dysplasia'
|
Hypospadias
|
Hypospadias 1, X-Linked
|
Hypothalamic Hamartomas
|
Hypothyroidism, Congenital, Nongoitrous, 2
|
Hypothyroidism, Congenital, Nongoitrous, 5
|
Hypotrichosis-Lymphedema-Telangiectasia Syndrome
|
Hypotrichosis Simplex
|
Hypoxia-Ischemia, Brain
|
Ichthyosis
|
Idiopathic Hypogonadotropic Hypogonadism
|
Iga Deficiency
|
Immune Dysregulation, Polyendocrinopathy, Enteropathy, X-Linked Syndrome
|
Immunologic Deficiency Syndromes
|
Inflammatory Bowel Disease 14
|
Insulinoma
|
Intestinal Diseases
|
Intestinal Polyps
|
Iridogoniodysgenesis, Dominant Type
|
Iridogoniodysgenesis Type1
|
Ischemic Attack, Transient
|
Ischiopatellar Dysplasia
|
Jaundice, Neonatal
|
Job Syndrome
|
Joint Diseases
|
Joint Instability
|
Juvenile Polyposis Syndrome
|
Juvenile Polyposis With Hereditary Hemorrhagic Telangiectasia
|
Kabuki Syndrome
|
Kallmann Syndrome
|
Keratitis, Hereditary
|
Keratoconus 1
|
Kyphosis
|
Lacrimal Apparatus Diseases
|
Lactose Intolerance, Adult Type
|
Langer-Giedion Syndrome
|
Langer Mesomelic Dysplasia
|
Laron Syndrome Type 2
|
Leigh Syndrome , French Canadian Type
|
Leiomyosarcoma
|
Leprosy
|
Leri-Weil Syndrome
|
Leukemia, Large Granular Lymphocytic
|
Leukemia, Myeloid, Chronic, Atypical, Bcr-Abl Negative
|
Leukostasis
|
Lewy Body Dementia
|
Li-Fraumeni Syndrome
|
Lig4 Syndrome
|
Limb-Mammary Syndrome
|
Lipoblastoma
|
Lipodystrophy, Familial Partial
|
Liposarcoma
|
Lissencephaly, X-Linked, 2
|
Lithiasis
|
Liver Failure, Acute
|
Furlong Syndrome
|
Long Qt Syndrome 11
|
Lower Extremity Deformities, Congenital
|
Lubs X-Linked Mental Retardation Syndrome
|
Interstitial Lung Disease
|
Lymphangioleiomyomatosis
|
Lymphatic Abnormalities
|
Lymphedema
|
Lymphedema Distichiasis Syndrome
|
Lymphedema, Hereditary, Ii
|
Lymphoma, Mantle-Cell
|
Colorectal Cancer, Hereditary Nonpolyposis, Type 1
|
Macrocytosis, Familial
|
Age-Related Macular Degeneration
|
Major Affective Disorder 1
|
Major Affective Disorder 7
|
Mandibulofacial Dysostosis, Treacher Collins Type, Autosomal Recessive
|
Manganese Poisoning
|
Marfan Syndrome
|
Marie Unna Congenital Hypotrichosis
|
Mason-Type Diabetes
|
Massive Hepatic Necrosis
|
Mastocytosis
|
Maturity-Onset Diabetes Of The Young, Type 1
|
Maturity-Onset Diabetes Of The Young, Type 3
|
Maturity-Onset Diabetes Of The Young, Type 4
|
Maturity-Onset Diabetes Of The Young, Type 7
|
Maturity-Onset Diabetes Of The Young, Type 9
|
Meacham Syndrome
|
Megalencephaly
|
Megalocytic Interstitial Nephritis
|
Melanoma Astrocytoma Syndrome
|
Melanoma, Experimental
|
Melanoma-Pancreatic Cancer Syndrome
|
Melas Syndrome
|
Melorheostosis
|
Meningioma, Familial
|
Meningitis, Aseptic
|
Meningomyelocele
|
Mental Disorders
|
Mental Retardation, Autosomal Dominant 1
|
Mental Retardation, Autosomal Recessive 3
|