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61
|
|
|
WASP actin nucleation promoting factor |
IMD2, SCNX, THC, THC1, WASP, WASPA |
Anemia, Arthritis, Chronic obstructive pulmonary disease, Congenital hypoplasia of thymus, Congenital neutropenia, Congenital thrombocytopenia, Conjunctivitis, Eczema, Hematomas, Hyperostosis, Immunologic deficiency syndromes, Iron deficiency anemia, Keratitis, Kidney disease, Leukemia, Lymphoma, Lymphopenia, Nervous system diseases, Neutropenia, Otitis media, Renal glomerular disease, Severe congenital neutropenia, x-linked, Sinusitis, Small vessel vasculitis, Specific learning disorder, Thrombocytopenia, Thrombocytopenia with normal platelets, x-linked, Thrombocytopenia, x-linked, Urticaria, Vasculitis, Wiskott-aldrich syndromeView all (16 more) |
|
62
|
|
|
WAS/WASL interacting protein family member 1 |
PRPL-2, WAS2, WASPIP, WIP |
Anemia, Arthritis, Atrial fibrillation, Chronic obstructive pulmonary disease, Congenital hypoplasia of thymus, Conjunctivitis, Eczema, Hematomas, Hyperostosis, Immunologic deficiency syndromes, Keratitis, Kidney disease, Leukemia, Lymphoma, Lymphopenia, Nervous system diseases, Neutropenia, Otitis media, Paroxysmal atrial fibrillation, Renal glomerular disease, Sinusitis, Specific learning disorder, Urticaria, Vasculitis, Wiskott-aldrich syndromeView all (10 more) |
|
63
|
|
|
WEE1 G2 checkpoint kinase |
WEE1A, WEE1hu |
|
|
64
|
|
|
Wolframin ER transmembrane glycoprotein |
CTRCT41, WFRS, WFS, WFSL |
Anemia, Anxiety disorder, Arachnodactyly, Ataxia, Autism, Bipolar disorder, Cardiomyopathy, Cataract, Cerebellar ataxia, Cerebral atrophy, Cerebral cortical atrophy, Congenital sensorineural hearing loss, Dandy-walker syndrome, Deafness, Dementia, Developmental delay, Developmental regression, Diabetes insipidus, Diabetes mellitus, Diaphragmatic eventration, Disorder of eye, Dysarthria, Dysautonomia, Dysphagia, Dyssomnia, Gastric ulcer, Glaucoma, Hallucinations, Hearing loss, Hydronephrosis, Hypothyroidism, Kidney disease, Laryngomalacia, Malabsorption syndrome, Mental depression, Mental retardation, Microglossia, Micrognathism, Mood disorder, Myopathy, Nervous system diseases, Neurogenic urinary bladder, Non-syndromic sensorineural deafness, Nyctalopia, Nystagmus, Optic atrophy, Peripheral axonal neuropathy, Psychosis, Ptosis, Retinitis pigmentosa, Sideroblastic anemia, Sleep apnea, Sleep disorders, Testicular atrophy, Testicular hypogonadism, Uranostaphyloschisis, Wolfram syndrome, Wolfram-like syndromeView all (43 more) |
|
65
|
|
|
- |
PRDS |
Absence of septum pellucidum, Axenfeld anomaly, Congenital anomaly of eye, Congenital clubfoot, Congenital epicanthus, Rib fusion, 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, Rieger syndrome, Scoliosis, Stenosis of external auditory canal, Stereotyped behavior, Strabismus, Ventricular septal defect, Wolf-hirschhorn syndromeView all (15 more) |
|
66
|
|
|
Wnt family member 1 |
BMND16, INT1, OI15 |
|
|
67
|
|
|
Wnt family member 2 |
INT1L1, IRP |
|
|
68
|
|
|
Wnt family member 3 |
INT4, TETAMS |
Agenesis of corpus callosum, Atresia of vagina, Atrial fibrillation, Bladder exstrophy and epispadias complex, Breast carcinoma, Cataract, Celiac disease, Choanal atresia, Adrenal gland agenesis, Asplenia, Congenital coloboma of iris, Pulmonary hypoplasia, Cryptorchidism, Gastroschisis, Hydrocephalus, Imperforate anus, Lung diseases, Malignant lymphoma, lymphocytic, intermediate differentiation, Lymphoma, lymphocytic, intermediate, Malignant mesothelioma, Mental depression, Microcornea, Micrognathism, Microphthalmos, Microstomia, Microtia, Mood disorder, Multicystic renal dysplasia, Optic atrophy, Oral cleft, Parkinson disease, Paroxysmal atrial fibrillation, Biliary cirrhosis, Renal agenesis, Septo-optic dysplasia, Tetraamelia, Tetraamelia syndrome, Tracheal stenosis, Urethral atresiaView all (24 more) |
|
69
|
|
|
Wnt family member 5A |
hWNT5A |
Accessory kidney, Alopecia, Anodontia, Avascular necrosis of the capital femoral epiphysis, Brachydactyly, Camptodactyly of fingers, Uterine cervix neoplasm, Cervical cancer, Clinodactyly, Congenital epicanthus, Congenital euryblepharon, Congenital exomphalos, Congenital hypoplasia of penis, Congenital pectus carinatum, Congenital pectus excavatum, Cryptorchidism, Developmental delay, Diffuse interstitial pulmonary fibrosis, Dwarfism, Epispadias, Female urogenital diseases, Fingernail dysplasia, Frontal bossing, Hernia, femoral, High palate, Hydronephrosis, Hypodontia, Hypospadias, Legg-calve-perthes disease, Lung neoplasms, Lung cancer, Macrocephaly, Macroglossia, Mental retardation, Mesomelia, Micrognathism, Micromelia, Oligodontia, Penis agenesis, Phakomatosis pigmentovascularis, Posteriorly rotated ear, Proptosis, Ptosis, Pulmonary fibrosis, Robinow syndrome, Scoliosis, Specific learning disorder, Strabismus, Strawberry nevus of skin, Syndactyly of fingersView all (35 more) |
|
70
|
|
|
Wnt family member 6 |
- |
|
