|
Craniofacial Abnormalities
|
|
Liver Cirrhosis, Experimental
|
|
Hepatocellular Carcinoma
|
|
Breast Carcinoma
|
|
Colorectal Cancer
|
|
Heart Defects, Congenital
|
|
Autism
|
|
Mesothelioma, Malignant
|
|
Female Urogenital Diseases
|
|
Cleft Lip
|
|
Ovarian Neoplasms
|
|
Glioblastoma Multiforme
|
|
Peritoneal Neoplasms
|
|
Medulloblastoma
|
|
Pheochromocytoma
|
|
Melanoma
|
|
Mesothelioma
|
|
Rheumatoid Arthritis
|
|
Inflammation
|
|
Intellectual Disability
|
|
Cell Transformation, Neoplastic
|
|
Prostatic Neoplasms
|
|
Kidney Disease
|
|
Carcinoma, Adenoid Cystic
|
|
Limb Deformities, Congenital
|
|
Liver Cirrhosis
|
|
Salivary Gland Neoplasm
|
|
Nervous System Malformations
|
|
Hernia, Diaphragmatic
|
|
Liver Neoplasms
|
|
Lung Diseases
|
|
Clubfoot
|
|
Coma
|
|
Congenital Abnormalities
|
|
Congenital Central Hypoventilation Syndrome
|
|
Currarino Triad
|
|
Cysts
|
|
Deafness, Autosomal Dominant 10
|
|
Deafness, Autosomal Recessive 67
|
|
Deafness, Congenital, With Inner Ear Agenesis, Microtia, And Microdontia
|
|
Diabetes Mellitus
|
|
Diabetes Mellitus, Type 2
|
|
Digeorge Syndrome
|
|
Disease Models, Animal
|
|
Drug-Induced Liver Injury
|
|
Dyskinesia, Drug-Induced
|
|
Limb Dystonia
|
|
Endometrial Neoplasm
|
|
Endometriosis
|
|
Epilepsy, Idiopathic Generalized
|
|
Esophageal Squamous Cell Carcinoma
|
|
Facial Palsy, Congenital, Unilateral Or Bilateral
|
|
Familial Medullary Thyroid Carcinoma
|
|
Fatty Liver
|
|
Fetal Death
|
|
Fetal Diseases
|
|
Gastrointestinal Stromal Tumors
|
|
Hand Foot Uterus Syndrome
|
|
Head And Neck Neoplasms
|
|
Hearing Loss, Conductive
|
|
Hearing Loss, Sensorineural
|
|
Heart Diseases
|
|
Heart Failure
|
|
Hepatitis
|
|
Hereditary Renal Agenesis
|
|
Hirschsprung Disease
|
|
Hodgkins Lymphoma
|
|
Huntington Disease
|
|
Hypercalcemia
|
|
Hypereosinophilic Syndrome
|
|
Hyperkinesis
|
|
Hyperparathyroidism
|
|
Hyperparathyroidism, Neonatal Severe Primary
|
|
Hypertension
|
|
Hypocalcemia
|
|
Hypocalciuric Hypercalcemia, Familial, Type 1
|
|
Hypoparathyroidism
|
|
Hypoparathyroidism Familial Isolated
|
|
Hypotension
|
|
Hypothermia
|
|
Hypothyroidism
|
|
Hypothyroidism, Congenital, Nongoitrous, 2
|
|
Hypothyroidism, Congenital, Nongoitrous, 4
|
|
Iridogoniodysgenesis, Dominant Type
|
|
Kallmann Syndrome
|
|
Kidney Failure, Chronic
|
|
Learning Disorders
|
|
Leukemia
|
|
Leukemia-Lymphoma, Adult T-Cell
|
|
Liver Diseases
|
|
Liver Failure, Acute
|
|
Lung Injury
|
|
Mammary Neoplasms, Animal
|
|
Mammary Neoplasms, Experimental
|
|
Manganese Poisoning
|
|
Movement Disorder
|
|
Multiple Endocrine Neoplasia
|
|
Multiple Endocrine Neoplasia Type 2a
|
|
Multiple Endocrine Neoplasia Type 2b
|
|
Multiple Sclerosis
|
|
Myocardial Ischemia
|
|
Necrosis
|
|
Neoplasm Invasiveness
|
|
Neoplasm Metastasis
|
|
Neoplasms, Experimental
|
|
Neoplasms, Germ Cell And Embryonal
|
|
Nerve Degeneration
|
|
Nervous System Diseases
|
|
Neuropathic Pain
|
|
Neural Tube Defects
|
|
Neuroblastoma
|
|
Neurogenic Inflammation
|
|
Obesity
|
|
Otofaciocervical Syndrome
|
|
Parkinsonian Disorders
|
|
Peripheral Demyelinating Neuropathy, Central Dysmyelination, Waardenburg Syndrome, And Hirschsprung Disease
|
|
Peters Anomaly
|
|
Polycystic Kidney, Autosomal Dominant
|
|
Polycystic Kidney Diseases
|
|
Polycystic Ovary Syndrome
|
|
Preaxial Deficiency, Postaxial Polydactyly And Hypospadias
|
|
Precancerous Conditions
|
|
Precursor B-Cell Lymphoblastic Leukemia-Lymphoma
|
|
Acute Lymphoblastic Leukemia
|
|
Protoporphyria, Erythropoietic
|
|
Pulmonary Fibrosis
|
|
Radioulnar Synostosis With Amegakaryocytic Thrombocytopenia
|
|
Reperfusion Injury
|
|
Respiratory System Abnormalities
|
|
Retinitis Pigmentosa 30
|
|
Rhabdomyosarcoma, Alveolar
|
|
Ring Dermoid Of Cornea
|
|
Schwannomatosis
|
|
Segawa Syndrome, Autosomal Recessive
|
|
Silicosis
|
|
Simpson-Golabi-Behmel Syndrome
|
|
Skin Abnormalities
|
|
Skin Diseases
|
|
Spinal Dysraphism
|
|
Status Epilepticus
|
|
Stomach Neoplasms
|
|
Stomatognathic Diseases
|
|
Drug Dependence
|
|
Testicular Germ Cell Tumor
|
|
Thrombosis
|
|
Thyroid Cancer, Follicular
|
|
Thyroid Cancer, Medullary
|
|
Thyroid Carcinoma
|
|
Tooth Abnormalities
|
|
Urinary Bladder Neoplasms
|
|
Waardenburg Syndrome Type 2
|
|
Waardenburg Syndrome, Type 4c
|
|
Weight Gain
|
|
Nephroblastoma
|
|
Wittwer Syndrome
|
|
22q11 Deletion Syndrome
|
|
Yemenite Deaf-Blind Hypopigmentation Syndrome
|
|
Abnormalities, Multiple
|
|
Acth Deficiency, Isolated
|
|
Alcohol Dependence
|
|
Amphetamine-Related Disorders
|
|
Amyloidosis, Familial
|
|
Amyotrophic Lateral Sclerosis 1
|
|
Arsenic Poisoning
|
|
Athabaskan Brainstem Dysgenesis
|
|
Autoimmune Diseases Of The Nervous System
|
|
Bamforth Syndrome
|
|
Barakat Syndrome
|
|
Biliary Tract Neoplasms
|
|
Bipolar Disorder
|
|
Bone Diseases, Developmental
|
|
Brain Diseases
|
|
Brain Ischemia
|
|
Branchio-Oto-Renal Syndrome
|
|
Burkitt Lymphoma
|
|
Cadmium Poisoning
|
|
Carcinoma
|
|
Carcinoma, Medullary
|
|
Carcinoma, Non-Small-Cell Lung
|
|
Dilated Cardiomyopathy
|
|
Cardiomyopathy, Dilated, 1j
|
|
Cardiovascular Abnormalities
|
|
Catalepsy
|
|
Cayler Cardiofacial Syndrome
|
|
Chondrosarcoma, Mesenchymal
|
|
Chordoma
|
|
Cirrhosis, Familial
|
