Craniofacial Abnormalities
|
Breast Carcinoma
|
Prostatic Neoplasms
|
Liver Cirrhosis, Experimental
|
Abortion, Spontaneous
|
Colorectal Cancer
|
Hypertension
|
Osteoarthritis
|
Rheumatoid Arthritis
|
Bone Diseases, Developmental
|
Liver Cirrhosis
|
Neoplasm Invasiveness
|
Limb Deformities, Congenital
|
Stomach Neoplasms
|
Lung Neoplasms
|
Hepatocellular Carcinoma
|
Uremia
|
Endometriosis
|
Autism
|
Melanoma
|
Pulmonary Fibrosis
|
Hernia, Diaphragmatic
|
Osteoporosis
|
Calcinosis
|
Kidney Disease
|
Neoplasm Metastasis
|
Adenocarcinoma
|
Cell Transformation, Neoplastic
|
Squamous Cell Carcinoma
|
Growth Disorders
|
Intellectual Disability
|
Heart Defects, Congenital
|
Glioblastoma Multiforme
|
Carcinoma, Non-Small-Cell Lung
|
Eye Abnormalities
|
Inflammation
|
Myocardial Ischemia
|
Pancreatic Carcinoma
|
Female Urogenital Diseases
|
Liver Neoplasms
|
Carcinoma, Adenoid Cystic
|
Cleft Lip
|
Adenoma
|
Mammary Neoplasms, Experimental
|
Skin Neoplasms
|
Asthma
|
Mesothelioma, Malignant
|
Mouth Neoplasms
|
Acute Kidney Injury
|
Diabetes Mellitus, Experimental
|
Carcinoma
|
Salivary Gland Neoplasm
|
Aortic Valve Insufficiency
|
Urinary Bladder Neoplasms
|
Nerve Degeneration
|
Drug-Induced Liver Injury
|
Colonic Neoplasm
|
Hyperalgesia
|
Obesity
|
Fibrosis
|
Oral Submucous Fibrosis
|
Bone Resorption
|
Tooth Abnormalities
|
Focal Segmental Glomerulosclerosis
|
Medulloblastoma
|
Thoracic Aortic Aneurysm
|
Keloid
|
Ovarian Neoplasms
|
Ureteral Obstruction
|
Liver Diseases
|
Mammary Neoplasms, Animal
|
Carcinoma, Squamous Cell Of Head And Neck
|
Rickets
|
Reperfusion Injury
|
Osteochondrodysplasias
|
Lung Diseases
|
Alcoholic Liver Cirrhosis
|
Furlong Syndrome
|
Carcinoma, Transitional Cell
|
Hypercalcemia
|
Aneurysm, Dissecting
|
Astrocytoma
|
Left Ventricular Hypertrophy
|
Heart Valve Diseases
|
Endometrial Neoplasm
|
Hearing Loss, Sensorineural
|
Muscular Atrophy
|
Infarction, Middle Cerebral Artery
|
Hyperplasia
|
Hand Deformities, Congenital
|
Aberrant Crypt Foci
|
Acromegaly
|
Hyperparathyroidism, Secondary
|
Arthritis, Experimental
|
Osteogenesis Imperfecta, Type 2a
|
Osteogenesis Imperfecta, Type 3
|
Osteogenesis Imperfecta, Type 4
|
Osteolysis
|
Edema
|
Osteoporosis, Postmenopausal
|
Osteosarcoma
|
Alzheimer's Disease
|
Psoriatic Arthritis
|
Ehlers-Danlos Syndrome Type 1
|
Chondrosarcoma
|
Ehlers-Danlos Syndrome, Type Vii, Autosomal Dominant
|
Parkinson's Disease
|
Aspirin Induced Asthma
|
Idiopathic Hypogonadotropic Hypogonadism
|
Endomyocardial Fibrosis
|
Anemia
|
Intervertebral Disc Disease
|
Intestinal Neoplasms
|
Polycystic Ovary Syndrome
|
Acth-Secreting Pituitary Adenoma
|
Kallmann Syndrome
|
Abnormalities, Multiple
|
Adrenal Gland Neoplasms
|
Kidney Failure, Chronic
|
Exostoses, Multiple Hereditary
|
Premature Birth
|
Adrenocortical Carcinoma
|
Lead Poisoning
|
Aortic Aneurysm
|
Uterine Fibroid
|
Crohn's Disease
|
Basal Cell Carcinoma
|
Puberty, Precocious
|
Chronic Obstructive Pulmonary Disease
|
Pulmonary Emphysema
|
Leukemia, Promyelocytic, Acute
|
Lewy Body Dementia
|
Autism Spectrum Disorder
|
Respiratory Distress Syndrome, Adult
|
Retinal Diseases
|
Liver Neoplasms, Experimental
|
Foot Deformities, Congenital
|
Schizophrenia
|
Fractures, Bone
|
Sepsis
|
Cardiac Hypertrophy
|
Autoimmune Disease
|
Cardiovascular Abnormalities
|
Glioma
|
Marfan Syndrome
|
Megaepiphyseal Dwarfism
|
Cartilage Diseases
|
Mesothelioma
|
Dermatitis, Allergic Contact
|
Beckwith-Wiedemann Syndrome
|
Multiple Myeloma
|
Cardiomyopathy, Dilated, 3b
|
Stroke
|
Muscular Dystrophy, Facioscapulohumeral
|
Musculoskeletal Abnormalities
|
Substance Withdrawal Syndrome
|
Heart Failure
|
Myocardial Infarction
|
Myopia
|
Aortic Rupture
|
Diabetes Mellitus, Type 2
|
Hemochromatosis
|
Neoplasms
|
Tetralogy Of Fallot
|
Bone Diseases
|
Diabetic Neuropathies
|
Hepatoblastoma
|
Disease Progression
|
Nephrotic Syndrome
|
Neurobehavioral Manifestations
|
Uterine Cervical Neoplasms
|
Acute Lung Injury
|
Uveal Melanoma
|
Ventricular Remodeling
|
Hypercholesterolemia
|
Hyperglycemia
|
Hyperinsulinism
|
Cholangitis
|
Nephroblastoma
|
Brachydactyly
|
Hypocalcemia
|
Hypochondroplasia
|
Hypoglycemia
|
Hypoparathyroidism Familial Isolated
|
Hypophosphatasia, Adult
|
Hypophosphatasia, Childhood
|
Hypophosphatasia, Infantile
|
Hypotension
|
Infertility
|
Male Infertility
|
Inflammatory Bowel Disease
|
Insulin-Like Growth Factor I Deficiency
|
Insulin Resistance
|
Intervertebral Disc Degeneration
|
Intestinal Polyps
|
Iridogoniodysgenesis Type1
|
Jackson-Weiss Syndrome
|
Jansen Type Metaphyseal Chondrodysplasia
|
Joint Instability
|
Keratoacanthoma Familial
|
Kidney Stone
|
Kniest Dysplasia
|
Kyphosis
|
Lacrimoauriculodentodigital Syndrome
|
Langer-Giedion Syndrome
|
Langer Mesomelic Dysplasia
|
Legg-Calve-Perthes Disease
|
Leopard Syndrome
|
Leri-Weil Syndrome
|
Chronic Lymphocytic Leukemia
|
Leukemia-Lymphoma, Adult T-Cell
|
Leukemia, Myeloid, Accelerated Phase
|
Leukemia, Myeloid, Acute
|
Leukemia, Myelomonocytic, Juvenile
|
Limb-Mammary Syndrome
|
Liver Diseases, Parasitic
|
Liver Failure, Acute
|
Lower Extremity Deformities, Congenital
|
Lupus Nephritis
|
Lymphangioleiomyomatosis
|
Lymphatic Metastasis
|
Lymphedema Distichiasis Syndrome
|
Lymphedema, Hereditary, Ii
|
Lymphoma, Mantle-Cell
|
Malignant Hyperthermia Susceptibility Type 5
|
Mandibuloacral Dysplasia With Type A Lipodystrophy
|
Mandibulofacial Dysostosis
|
Mass Syndrome
|
Memory Disorders
|
Metaphyseal Anadysplasia 2
|
Metaphyseal Chondrodysplasia Schmid Type
|
Microphthalmia, Syndromic 6
|
Mitral Valve Prolapse
|
Morphine Dependence
|
Muenke Syndrome
|
Multiple Organ Failure
|
Muscular Diseases
|
Myelodysplastic Syndromes
|
Myeloproliferative Disorder
|
Myocardial Reperfusion Injury
|
Nasopharyngeal Neoplasm
|
Necrosis
|
Neointima
|
Neoplasms, Experimental
|
Neoplasms, Germ Cell And Embryonal
|
Neoplasms, Squamous Cell
|
Neovascularization, Pathologic
|
Nephritis
|
Nephrocalcinosis
|
Nephrogenic Fibrosing Dermopathy
|
Nephrosis
|
Nervous System Diseases
|
Neuroblastoma
|
Neuroendocrine Tumors
|
Multiple Synostoses Syndrome 1
|
Non-Alcoholic Fatty Liver Disease
|
Noonan Syndrome
|
No-Reflow Phenomenon
|
Occupational Diseases
|
Oral Ulcer
|
Orofacial Cleft 11
|
Osseous Heteroplasia, Progressive
|
Ossification, Heterotopic
|
Osteoarthritis With Mild Chondrodysplasia
|
Osteogenesis Imperfecta
|
Osteoglophonic Dwarfism
|
Osteomalacia
|
Osteosclerosis
|
Ovarian Cysts
|
Pain
|
Pancreatitis, Acute Necrotizing
|
Pancreatitis, Alcoholic
|
Pancreatitis, Chronic
|
Papilloma
|
Paralysis
|
Parietal Foramina
|
Parietal Foramina 2
|
Penile Induration
|
Peptic Ulcer
|
Periodontitis
|
Peripheral Arterial Disease
|
Peripheral Neuropathy
|
Peritoneal Fibrosis
|
Peritoneal Neoplasms
|
Pfeiffer Type Acrocephalosyndactyly
|
Pierre Robin Syndrome
|
Pierre Robin Syndrome With Fetal Chondrodysplasia
|
Pilomatrixoma
|
Pituitary Neoplasms
|
Placenta Diseases
|
Platelet Disorder, Familial, With Associated Myeloid Malignancy
|
Platyspondylic Lethal Skeletal Dysplasia, Torrance Type
|
Pleural Diseases
|
Pneumoconiosis
|
Pneumonia
|
Polydactyly
|
Polyhydramnios
|
Port-Wine Stain
|
Potocki-Lupski Syndrome
|
Preaxial Deficiency, Postaxial Polydactyly And Hypospadias
|
Precancerous Conditions
|
Precursor B-Cell Lymphoblastic Leukemia-Lymphoma
|
Acute Lymphoblastic Leukemia
|
Preeclampsia
|
Prolactinoma
|
Propping Zerres Syndrome
|
Prostatic Intraepithelial Neoplasia
|
Proteinuria
|
Pseudoachondroplasia
|
Pseudohypoaldosteronism
|
Pseudohypoparathyroidism
|
Pseudohypoparathyroidism Type 1b
|
Pseudopseudohypoparathyroidism
|
Psychomotor Agitation
|
Psychomotor Disorders
|
Radioulnar Synostosis With Amegakaryocytic Thrombocytopenia
|
Raine Syndrome
|
Rapadilino Syndrome
|
Rapp-Hodgkin Syndrome
|
Rectum Cancer
|
Renal Insufficiency
|
Respiration Disorders
|
Respiratory Insufficiency
|
Respiratory System Abnormalities
|
Retinal Detachment
|
Rhabdomyosarcoma
|
Robinow Syndrome, Autosomal Recessive
|
Rothmund-Thomson Syndrome
|
Sandhoff Disease
|
Sarcoidosis
|
Schistosomiasis
|
Systemic Scleroderma
|
Scoliosis
|
Seizures
|
Seminoma
|
Sexual Dysfunction, Physiological
|
Short Stature, Idiopathic, Autosomal
|
Short Stature, Idiopathic, X-Linked
|
Shprintzen Golberg Craniosynostosis
|
Silver-Russell Syndrome
|
Situs Inversus
|
Skeletal Defects, Genital Hypoplasia, And Mental Retardation
|
Skin Abnormalities
|
Small Cell Lung Carcinoma
|
Smith-Magenis Syndrome
|
Spinocerebellar Ataxias
|
Split-Hand-Foot Malformation 4
|
Spondylarthritis
|
Spondyloepimetaphyseal Dysplasia, Aggrecan Type
|
Spondyloepimetaphyseal Dysplasia, Matrilin-3 Related
|
Spondylodysplasia And Premature Pubarche
|
Spondyloepiphyseal Dysplasia, Congenita
|
Spondyloepiphyseal Dysplasia, Kimberley Type
|
Spondylo-Megaepiphyseal-Metaphyseal Dysplasia
|
Spondylometaphyseal Dysplasia, Kozlowski Type
|
Status Epilepticus
|
Toxic Epidermal Necrolysis
|
Stickler Syndrome, Type 1
|
Stickler Syndrome, Type 3
|
Stickler Syndrome, Type I, Nonsyndromic Ocular
|
Stiff Skin Syndrome
|
Stomach Ulcer
|
Stomatognathic Diseases
|
Stomatognathic System Abnormalities
|
Strudwick Syndrome
|
Sturge-Weber Syndrome
|
Subarachnoid Hemorrhage
|
Superior Vena Cava Syndrome
|
Progressive Supranuclear Palsy
|
Sweat Gland Neoplasms
|
Syndactyly
|
Syndactyly, Type V
|
Synovitis
|
Synpolydactyly 1
|
Tachycardia
|
Tay-Sachs Disease
|
Ter Haar Syndrome
|
Testicular Germ Cell Tumor
|
Thanatophoric Dysplasia, Type 2
|
Thanatophoric Dysplasia
|
Thrombocythemia, Essential
|
Thyroid Diseases
|
Trichorhinophalangeal Syndrome, Type I
|
Trichorhinophalangeal Syndrome, Type Iii
|
Turcot Syndrome
|
Ulnar-Mammary Syndrome
|
Urinary Bladder, Overactive
|
Urinary Retention
|
Urogenital Abnormalities
|
Urticaria
|
Uterine Neoplasms
|
Vater Association
|
Vertical Talus, Congenital
|
Vitamin A Deficiency
|
Vitamin D Deficiency
|
Rickets, Hereditary Vitamin D-Resistant
|
Weight Gain
|
Weight Loss
|
Weill-Marchesani Syndrome
|
Weyers Acrofacial Dysostosis
|
Wolcott-Rallison Syndrome
|
Yellow Nail Syndrome
|
Achondrogenesis Type 2
|
Achondroplasia
|
Acrocapitofemoral Dysplasia
|
Acromicric Dysplasia
|
Acute Coronary Syndrome
|
Lung Adenocarcinoma
|
Adenoma, Liver Cell
|
Adenomatous Polyposis Coli
|
Adenomatous Polyps
|
Albright's Hereditary Osteodystrophy
|
Albuminuria
|
Androgenetic Alopecia
|
Alveolar Bone Loss
|
Amelogenesis Imperfecta
|
Angina, Stable
|
Anodontia
|
Anonychia Congenita
|
Anoxia
|
Anxiety Disorder
|
Aortic Diseases
|
Arachnodactyly
|
Cardiac Arrhythmia
|
Arthritis
|
Arthritis, Juvenile
|
Asbestosis
|
Asthma, Nasal Polyps, And Aspirin Intolerance
|
Asthma, Occupational
|
Atherosclerosis
|
Atrial Fibrillation
|
Atrial Fibrillation, Familial 1
|
Atrial Septal Defect 6
|
Atrial Standstill
|
Auditory Neuropathy, Autosomal Dominant, 1
|
Basal Cell Nevus Syndrome
|
Berylliosis
|
Blood Coagulation Disorders
|
Bone Diseases, Endocrine
|
Bone Diseases, Metabolic
|
Bone Neoplasms
|
Brachydactyly-Syndactyly Syndrome
|
Brachydactyly Type A1
|
Brachydactyly Type A2
|
Brachydactyly, Type B1
|
Brachydactyly, Type D
|
Brachyolmia
|
Bradycardia
|
Brain Edema
|
Brain Injuries
|
Brain Ischemia
|
Branchio-Oto-Renal Syndrome
|
Breast Diseases
|
Bronchopulmonary Dysplasia
|
Cachexia
|
Cafe-Au-Lait Spots
|
Campomelic Dysplasia
|
Camurati-Engelmann Syndrome
|
Carcinoma, Pancreatic Ductal
|
Carcinosarcoma
|
Cardiomyopathies
|
Cardiovascular Disease
|
Cataract
|
Catshl Syndrome
|
Cecal Neoplasms
|
Intracerebral Hemorrhage
|
Cerebrovascular Disorders
|
Charcot-Marie-Tooth Disease
|
Charge Syndrome
|
Cholangiocarcinoma
|
Cholestasis
|
Chondrocalcinosis 2
|
Chondrodysplasia, Acromesomelic, With Genital Anomalies
|
Chondrodysplasia, Blomstrand Type
|
Chondrodysplasia Punctata 2, X-Linked Dominant
|
Chondrodysplasia Punctata, Brachytelephalangic
|
Chromosome 2q37 Deletion Syndrome
|
Cleidocranial Dysplasia
|
Clubfoot
|
Cocaine Dependence
|
Coffin-Lowry Syndrome
|
Cognitive Impairment
|
Colitis
|
Ulcerative Colitis
|
Colonic Polyps
|
Colorectal Neoplasms, Hereditary Nonpolyposis
|
Congenital Abnormalities
|
Copper-Overload Cirrhosis
|
Corneal Diseases
|
Craniometaphyseal Dysplasia, Autosomal Dominant
|
Craniopharyngioma
|
Craniosynostoses
|
Craniosynostosis Radial Aplasia Syndrome
|
Crouzon Syndrome With Acanthosis Nigricans
|
Cushing's Symphalangism
|
Cyanosis
|
Cystic Fibrosis
|
Dandy-Walker Syndrome
|
Deafness, Autosomal Dominant 13
|
Deafness, Autosomal Dominant 39, With Dentinogenesis Imperfecta 1
|
Deafness, Autosomal Recessive 53
|
Deafness, Congenital, With Inner Ear Agenesis, Microtia, And Microdontia
|
Demyelinating Diseases
|
Dentinogenesis Imperfecta
|
Dentinogenesis Imperfecta, Shields Type 3
|
Unipolar Depression
|
Dermatitis, Contact
|
Desmoid Disease, Hereditary
|
Diabetes Mellitus, Type 1
|
Diabetic Cardiomyopathies
|
Diabetic Nephropathy
|
Disease Models, Animal
|
Drug Hypersensitivity
|
Drug-Related Side Effects And Adverse Reactions
|
Dry Eye Syndromes
|
Duodenal Ulcer
|
Dyssomnias
|
Ectopia Lentis
|
Ectrodactyly-Cleft Lip-Palate Syndrome
|
Ectrodactyly, Ectodermal Dysplasia, And Cleft Lip-Palate Syndrome 3
|
Ehlers-Danlos Syndrome
|
Ehlers-Danlos Syndrome, Cardiac Valvular Form
|
Ehlers-Danlos Syndrome Type 3
|
Eiken Skeletal Dysplasia
|
Ellis-Van Creveld Syndrome
|
Enchondromatosis
|
Endocrine System Diseases
|
Endometrial Hyperplasia
|
Epidermal Nevus
|
Epilepsy, Temporal Lobe
|
Epiphyseal Dysplasia, Multiple, 1
|
Epiphyseal Dysplasia, Multiple, 2
|
Epiphyseal Dysplasia, Multiple, 5
|
Epiphyseal Dysplasia, Multiple, With Myopia And Conductive Deafness
|
Erectile Dysfunction
|
Erythema
|
Esophageal Neoplasms
|
Esophageal Squamous Cell Carcinoma
|
Eye Injuries
|
Failure Of Tooth Eruption, Primary
|
Familial Hypophosphatemic Rickets
|
Familial Primary Pulmonary Hypertension
|
Familial Testotoxicosis
|
Fatty Liver
|
Femoral Fractures
|
Femur Head Necrosis
|
Fetal Growth Retardation
|
Fibromatosis, Abdominal
|
Fibromatosis, Aggressive
|
Fibrous Dysplasia, Polyostotic
|
Gallstones
|
Gastrointestinal Diseases
|
Gastrointestinal Neoplasms
|
Genetic Diseases, Inborn
|
Glaucoma
|
Glaucoma, Primary Open Angle
|
Gliosis
|
Iga Glomerulonephritis
|
Growth Hormone-Secreting Pituitary Adenoma
|
Hand Foot Uterus Syndrome
|
Hay-Wells Syndrome
|
Hearing Loss
|
Heat Stroke
|
Hemangiosarcoma
|
Hemorrhagic Disorders
|
Hepatitis, Autoimmune
|
Hepatitis, Chronic
|
Hepatorenal Syndrome
|
Hernias, Diaphragmatic, Congenital
|
Heterotaxy Syndrome
|
Holoprosencephaly 9
|
Hyaloideoretinal Degeneration Of Wagner
|
Hypercalciuria
|
Hyperlipidemias
|
Hyperostosis
|
Hyperostosis, Cortical, Congenital
|
Hyperparathyroidism
|
Hyperphosphatemia
|
Allergy
|
Pulmonary Hypertension
|
Hypertrophy
|