192251
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- |
- |
Curated: N/A
Unreviewed: Addison`s Disease, Ankylosing Spondylitis, Arthritis, Autoimmune Diseases, Behcet Syndrome, Coffin-Siris Syndrome, Connective Tissue Disease, Crohn Disease, Cystic Fibrosis, Dermatomyositis, Diabetes Mellitus, Glomerulonephritis, Granulomatosis With Polyangiitis, Graves Disease, Hemophagocytic Syndrome, Henoch-Schonlein Nephritis, Inflammatory Myofibroblastic Tumor, Kawasaki disease, Laryngeal carcinoma, Lupus Erythematosus, Lupus Nephritis, Lupus Vulgaris, Lymphohistiocytosis, Lymphoma, Psoriasis, Rheumatoid arthritis, Rhinitis, Sarcoidosis, Small vessel vasculitis, T-Cell Lymphoma, Takayasu Arteritis, Ulcerative colitis, Uveal Melanoma, Vasculitis, Vitamin D Deficiency
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192252
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WASP homolog associated with actin, golgi membranes and microtubules |
WHAMM1, WHDC1 |
Curated: Premature ovarian failure
Unreviewed: Galloway-mowat syndrome, Leukemia, Periodontitis
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192253
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WHAMM pseudogene 1 |
WHDC1P1 |
Curated: N/A
Unreviewed: N/A
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192254
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WHAMM pseudogene 2 |
WHAMML2, WHDC1L2 |
Curated: N/A
Unreviewed: Hepatocellular carcinoma
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192255
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WHAMM pseudogene 3 |
WHAMML1, WHDC1L1 |
Curated: N/A
Unreviewed: Prader-Willi Syndrome
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192256
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WHAMM pseudogene 4 |
- |
Curated: N/A
Unreviewed: N/A
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192257
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- |
PRDS |
Curated: N/A
Unreviewed: Absence Of Septum Pellucidum, Axenfeld anomaly, Congenital anomaly of eye, Congenital Clubfoot, Congenital Epicanthus, Cryptorchidism, Developmental Delay, Dwarfism, Gastroesophageal Reflux Disease, Hemangioma, Hypodontia, Hypospadias, Immunologic Deficiency Syndromes, Mental retardation, Microcephaly, Micrognathism, Nystagmus, Pitt-Rogers-Danks Syndrome, Precocious puberty, Proptosis, Ptosis, Radioulnar Synostosis, Rib fusion, Rieger syndrome, Scoliosis, Stenosis Of External Auditory Canal, Stereotyped Behavior, Strabismus, Ventricular septal defect, Wolf-Hirschhorn Syndrome
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192258
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Winged helix repair factor 1 |
D6S60, D6S60E, G11, HLA-RP1, RP1, STK19, TWH19 |
Curated: Atrophic macular degeneration, Bullous pemphigoid, Basal cell carcinoma, Cervical cancer, Gastroesophageal reflux disease, Hypothyroidism, Major depressive disorder, Membranous glomerulonephritis, Rheumatoid arthritis, Sarcoidosis, Schizophrenia, Systemic lupus erythematosus, Upper aerodigestive tract neoplasm, Urticaria, Age-related macular degeneration
Unreviewed: Carcinoma, Diabetes Mellitus, Exudative Macular Degeneration, Geographic Atrophy, Lung adenocarcinoma, Lung Cancer, Lupus Erythematosus, Melanoma, Membranous Glomerulonephritis, Mental Depression, Multiple Sclerosis, Myasthenia Gravis, Pemphigus Vulgaris, Scleroderma, Skin carcinoma
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192259
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Winged helix repair factor 1B (pseudogene) |
RP2, STK19B, STK19P, bPG116M5.10 |
Curated: N/A
Unreviewed: N/A
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192260
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Whirlin |
CIP98, DFNB31, PDZD7B, USH2D, WI |
Curated: Isolated sensorineural deafness, Nonsyndromic hearing loss, Bipolar disorder, Deafness, Hearing loss, Hereditary hearing loss, Metabolic syndrome, Obesity, Ocular albinism, Ocular hypotension, Optic atrophy, Pancreatic cancer, Retinitis pigmentosa, Retinitis pigmentosa-deafness syndrome, Diabetes mellitus type 2, Usher syndrome, Usher syndrome type 2D, nonsyndromic genetic hearing loss
Unreviewed: Anxiety Disorder, Bipolar Disorder, Blindness, Cataract, Cerebral cortical atrophy, Ciliopathies, Colonic Neoplasms, Disorder Of Eye, Hallucinations, Hearing Loss, Hemianopsia, Hemochromatosis, Hereditary Retinal Dystrophy, Long qt syndrome, Mental Depression, Microdontia, Myopia, Non-Syndromic Sensorineural Deafness, Nonsyndromic Deafness, Nyctalopia, Nystagmus, Retinitis Pigmentosa, Rod-cone dystrophy, Schizophrenia, Subcortical cerebral atrophy, Usher Syndrome
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