921
|
|
|
SHOX homeobox |
GCFX, PHOG, SHOX1, SHOXY, SS |
Curated: Connective tissue disease, Desbuquois syndrome
Unreviewed: 2q37 Deletion Syndrome, Achondroplasia, Anterior segment dysgenesis, Aromatase Deficiency, Arthritis, Becker Muscular Dystrophy, Bone disease, Brachydactyly, Camptodactyly of fingers, Catshl syndrome, Clubfoot, Colorectal neoplasm, Congenital abnormalities, Congenital bone marrow failure syndrome, Congenital Chromosomal Disease, Congenital Hypoplasia Of Radius, Cubitus valgus, Developmental Delay, Disorders of sex development, Down Syndrome, Duchenne Muscular Dystrophy, Dwarfism, Dyslipidemias, Dysmorphic Features, Episodic ataxia, Estrogen Resistance, Generalized epilepsy, Gonadal Dysgenesis, Growth disorder, High palate, Hodgkin disease, Horizontal gaze palsy with progressive scoliosis, Hypertension, Hypertrophy, Hypochondroplasia, Hypogonadism, Hypoplasia Of Lower Limb, Hypospadias, Ichthyosis, Intervertebral Disc Degeneration, Isolated Somatotropin Deficiency, Kallmann Syndrome, Langer Mesomelic Dysplasia Syndrome, Leri-Weill Dyschondrosteosis, Lowry Wood Syndrome, Madelung deformity, Melanocytic nevus, Mesomelia, Micrognathism, Micromelia, Mucopolysaccharidosis, Multiple congenital exostosis, Muscular dystrophy, Non-obstructive azoospermia, Noonan Syndrome, Obesity, Osteochondrodysplasia, Osteosarcoma, Ovarian Failure, Pituitary dwarfism, Premature Menopause, Rickets, Scoliosis, SHORT STATURE, IDIOPATHIC, X-LINKED, Short syndrome, SHOX-Related Short Stature, Skeletal Dysplasia, Somatotropin Deficiency, Timothy Syndrome, Tourette Syndrome, Tracheoesophageal fistula, Tricuspid Valve Stenosis, Triglyceride Storage Disease With Ichthyosis, Tuberous Sclerosis, Turner Syndrome, Urogenital abnormalities
|
922
|
|
|
SHOX homeobox 2 |
OG12, OG12X, SHOT |
Curated: Atrial fibrillation, Basal cell carcinoma, Lung cancer, Major depressive disorder, Schizophrenia
Unreviewed: Astrocytoma, Atrial Fibrillation, Biliary tract neoplasms, Brain neoplasms, Breast Cancer, Breast Carcinoma, Breast neoplasm, Carcinogenesis, Cholangiocarcinoma, Colonic disease, Colonic neoplasm, Colorectal neoplasm, Cornelia De Lange Syndrome, Esophageal neoplasm, Esophagus Neoplasm, Glioblastoma, Glioma, Hematologic neoplasm, Hepatocellular carcinoma, Intervertebral Disc Degeneration, Langer Mesomelic Dysplasia Syndrome, Leri-Weill Dyschondrosteosis, Liver carcinoma, Lung Cancer, Lung carcinoma, Lung disease, Lung Diseases, Lung neoplasms, Lymphoma, Malignant Neoplasm, Melanoma, Mesothelioma, Multiple polyposis syndrome, Neoplasms, Neuroblastoma, Nonorganic Psychosis, Oestrogen Receptor Positive Breast Cancer, Pleural effusion, Prostate cancer, Psychosis, Renal Carcinoma, Sarcoidosis, Sarcoma, Sick sinus syndrome, Small cell lung carcinoma, Squamous cell carcinoma, Systemic sclerosis, Temporomandibular Joint Disorders
|
923
|
|
|
Sedoheptulokinase |
CARKL, SHK |
Curated: Sedoheptulokinase deficiency, Dementia
Unreviewed: Anemia, Arthrogryposis multiplex congenita, Cholestatic liver disease, Cystinosis, Deficiency Of Sedoheptulokinase, Diabetes mellitus, type 1, Dwarfism, Glioblastoma, Isolated Sedoheptulokinase Deficiency, Macrocephaly, Multiple sclerosis, Portal Hypertension, Postnatal asphyxia, Renal Insufficiency, Subcortical cerebral atrophy
|
924
|
|
|
SNF2 histone linker PHD RING helicase |
RAD5, bA545I5.2 |
Curated: Gastric cancer
Unreviewed: Glioblastoma, Glioma, Hepatocellular carcinoma, Liver carcinoma, Malignant Neoplasm, Neoplasms, Neuroblastoma
|
925
|
|
|
SHQ1, H/ACA ribonucleoprotein assembly factor |
DYT35, GRIM-1, NEDDS, Shq1p |
Curated: Diabetes mellitus, Dystonia, Torsion dystonia, Early-onset generalized limb-onset dystonia, Metabolic syndrome, Neurodevelopmental disorder, Diabetes mellitus type 2
Unreviewed: Anaplasia, Bone marrow failure syndrome, Dyskeratosis Congenita, Dyskeratosis Congenita, X-Linked, Head and neck cancer, Head And Neck Carcinoma, Hoyeraal hreidarsson syndrome, Lung carcinoma, Lymphoblastic Leukemia, Malignant Neoplasm, Neoplasms, Nervous System Disorder, Prostatic neoplasm, Prostatic Neoplasms
|
926
|
|
|
SHQ1, H/ACA ribonucleoprotein assembly factor pseudogene 1 |
- |
Curated: N/A
Unreviewed: N/A
|
927
|
|
|
Shroom family member 1 |
APXL2 |
Curated: Metabolic syndrome, Diabetes mellitus type 2
Unreviewed: Arthritis, Neural Tube Defect
|
928
|
|
|
Shroom family member 2 |
APXL, HSAPXL |
Curated: Colorectal cancer, Meniere disease, Prostate cancer
Unreviewed: Alzheimer disease, Breast Cancer, Colonic Neoplasms, Colorectal Cancer, Colorectal neoplasm, Colorectal Neoplasms, Nasopharyngeal Carcinoma, Neural Tube Defect, Neurofibromatosis, Ocular albinism
|
929
|
|
|
Shroom family member 2 pseudogene 1 |
APXLP |
Curated: N/A
Unreviewed: N/A
|
930
|
|
|
Shroom family member 3 |
APXL3, MSTP013, SHRM, ShrmL |
Curated: Alzheimer disease, Atrial fibrillation, Cholecystolithiasis, Kidney disease, Coronary artery disease, Craniofacial microsomia, Eosinophilia, Gallstones, Intrahepatic cholestasis of pregnancy, Metabolic syndrome, Myocardial infarction, Nephrolithiasis, Neural tube defect, Parkinson disease, Prostate cancer, Systemic lupus erythematosus, Tetralogy of fallot, Diabetes mellitus type 2, Urolithiasis
Unreviewed: Amyotrophic lateral sclerosis, Atrial Septal Defect, Cardiomyopathy, Cleft palate, Diabetes, Diabetes Mellitus, Diabetic neuropathy, Glioblastoma, Goldenhar Syndrome, Hearing loss, Heterotaxia, Heterotaxy syndrome, Kidney Disease, Kidney Failure, Kidney stone, Leukemia, Malignant Neoplasm, Neoplasms, Neural Tube Defect, Neuroblastoma, Orofacial cleft, Oropharyngeal neoplasm, Renal Insufficiency, Situs ambiguus
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