|
31
|
|
|
WD repeat domain 62 |
C19orf14, MCPH2 |
Agenesis of corpus callosum, Congenital microcephaly, Cortical dysplasia, Developmental delay, Dwarfism, Hypoplasia of corpus callosum, Mental retardation, Liver carcinoma, Malformation of cortical development, Microcephaly, Microlissencephaly, Neuronal heterotopia, Pachygyria, Polymicrogyria, Renal aplasia, Schizencephaly, Spastic tetraparesis, Vesicoureteral refluxView all (3 more) |
|
32
|
|
|
WD repeat domain 53 |
- |
|
|
33
|
|
|
WASP family member 5, pseudogene |
- |
|
|
34
|
|
|
WEE2 oocyte meiosis inhibiting kinase |
OOMD5, OZEMA5, WEE1B |
|
|
35
|
|
|
WD repeat containing planar cell polarity effector |
BBS15, C2orf86, CHDTHP, CPLANE5, FRITZ, FRTZ |
Anencephaly, Aortic coarctation, Asthma, Atrioventricular septal defect, Attention deficit hyperactivity disorder, Bardet-biedl syndrome, Benign neoplasm of nervous system, Cataract, Ciliopathies, Asplenia, Congenital cerebral hernia, Congenital hepatic fibrosis, Hypoplasia of the ovary, Congenital hypoplasia of penis, Cryptorchidism, Cystic liver disease, Dandy-walker syndrome, Disorder of eye, Double ureter, Dwarfism, Eczema, Fibrosis of pancreas, Foot polydactyly, Heart defect, tongue hamartoma and polysyndactyly, Hydrocephalus, Hypertension, Hypogonadism, Liver fibrosis, Lobar holoprosencephaly, Male pseudohermaphroditism, Malignant melanoma of skin, Meckel syndrome, Meckel-gruber syndrome, Melanoma, Mental retardation, Microcephaly, Microcornea, Micrognathism, Microphthalmos, Multicystic renal dysplasia, Nephrotic syndrome, Nystagmus, Obesity, Optic atrophy, Orstavik lindemann solberg syndrome, Pancreatic cyst, Patent ductus arteriosus, Polycystic liver disease, Polydactyly, Prostate cancer, Retinitis pigmentosa, Sclerocornea, Situs inversus, Speech disorders, Subaortic stenosis, Syndactyly of fingers, Syndromic microphthalmia, Talipes, True hermaphroditism, Postaxial hand polydactyly, Urethral atresiaView all (46 more) |
|
36
|
|
|
WW domain containing adaptor with coiled-coil |
BM-016, DESSH, PRO1741, Wwp4 |
10p12-p11 deletion syndrome, Alzheimer disease, Anxiety disorder, Astigmatism, Attention deficit hyperactivity disorder, Brachycephaly, Colorectal cancer, Congenital epicanthus, Desanto-shinawi syndrome, Developmental delay, Dysmorphic features, Facial dysmorphism-developmental delay-behavioral abnormalities syndrome, Mental retardation, Multiple congenital anomalies, Multiple myeloma, Myopia, Hypoglycemia, Neurodevelopmental disorders, Posteriorly rotated ear, Prostatic neoplasms, Prostate cancer, Strabismus, SynophrysView all (8 more) |
|
37
|
|
|
WT1 antisense RNA |
WIT-1, WIT1, WT1-AS1, WT1AS |
|
|
38
|
|
|
Wnt family member 16 |
- |
|
|
39
|
|
|
WW domain containing oxidoreductase |
D16S432E, DEE28, EIEE28, FOR, FRA16D, HHCMA56, PRO0128, SCAR12, SDR41C1, WOX1 |
46, xy partial gonadal dysgenesis, Alzheimer disease, Ambiguous genitalia, Arthritis, Spinocerebellar ataxia, Attention deficit hyperactivity disorder, Autism, Azoospermia, Benign neoplasm of esophagus, Brain atrophy, Breast cancer, Mammary neoplasms, Breast carcinoma, Carcinoma, Cerebellar ataxia, epilepsy, mental retardation, Cerebellar atrophy, Cerebral atrophy, Colonic neoplasms, Colorectal cancer, Colorectal neoplasms, Cryptorchidism, Developmental delay, Developmental regression, Dwarfism, Dysarthria, Dyskinetic syndrome, Epileptic encephalopathy, Esophageal carcinoma, Esophagus neoplasm, Gastric cancer, Gastroesophageal reflux disease, Gonadal dysgenesis, Gynecomastia, Hypertrophy of clitoris, Hypodontia, Hypogonadism, Hypoplasia of vagina, Hypospadias, Juvenile arthritis, Leukemia, Marfan syndrome, Mental retardation, Microcephaly, Motor delay, Multiple sclerosis, Nephroblastoma, Nephrotic syndrome, Non-specifi epileptic encephalopathy, Nystagmus, Obesity, Optic atrophy, Osteoporosis, Ovarian gonadoblastoma, Penis agenesis, Physiologic amenorrhea, Seronegative polyarthritis, Polyarthritis, rheumatoid factor positive, Ptosis, Senile dementia, Status epilepticus, Still disease, Stomach neoplasms, Streak ovary, Testicular gonadoblastoma, Testicular regression syndrome, Urinary tract cancer, Urologic neoplasms, Vascular diseasesView all (53 more) |
|
40
|
|
|
Wnt family member 4 |
SERKAL, WNT-4 |
Acne, Cubitus valgus, Brachydactyly, Adrenal gland agenesis, Congenital diaphragmatic hernia, Pulmonary hypoplasia, Dwarfism, Endometriosis, Female urogenital diseases, Hypospadias, Kidney disease, Mullerian aplasia and hyperandrogenism, Obesity, Oral cleft, Ovarian cancer, Ovarian epithelial carcinoma, Ovotestis, Physiologic amenorrhea, Prostatic neoplasms, Prostate cancer, Pulmonary stenosis, Renal agenesis, Serkal syndrome, Sex reversal, female, with dysgenesis of kidneys, adrenals, and lungs, Synophrys, True hermaphroditism, Uterine fibroids, Plexiform leiomyoma, Ventricular septal defectView all (14 more) |
