|
81
|
|
|
WD repeat domain 76 |
CDW14, CMR1 |
|
|
82
|
|
|
WW and C2 domain containing 2 |
BOMB |
|
|
83
|
|
|
WD repeat domain 26 |
CDW2, GID7, MIP2, SKDEAS |
Developmental delay, Dysmorphic features, Hypoplasia of corpus callosum, Intellectual disability-seizures-abnormal gait-facial dysmorphism syndrome, Mental retardation, Micrognathism, Multiple congenital anomalies, Otitis media, Skraban-deardorff syndrome, Sleep apnea, Strabismus |
|
84
|
|
|
WD repeat and coiled coil containing |
C2orf44, MMAP, PP384 |
|
|
85
|
|
|
Wnt family member 10A |
ECTD16, OODD, SSPS, STHAG4 |
Acne, Alopecia, Alopecia, male pattern, Androgenetic alopecia, Anodontia, Anonychia, Apocrine adenoma, Apocrine cystadenoma, Carcinoma, Dysmorphic features, Ectodermal dysplasia, Hyperhidrosis palmaris et plantaris, Hypodontia, Hypodontia oligodontia with orofacial cleft, Hypohidrosis, Hypohidrotic ectodermal dysplasia, Hypoplasia of teeth, Hypoplasia of the maxilla, Hypotrichosis, Keratosis pilaris, Malignant lymphoma, lymphocytic, intermediate differentiation, Lymphoma, lymphocytic, intermediate, Microdontia, Micrognathism, Nail diseases, Nail dysplasia, Odontoonychodermal dysplasia, Oligodontia, Onycholysis, Ovarian neoplasm, Palmoplantar keratoderma, Poroma, Schopf-schulz-passarge syndrome, Tooth agenesis, Tooth development and eruption disorderView all (20 more) |
|
86
|
|
|
WD repeat domain 82 |
MST107, MSTP107, PRO2730, PRO34047, SWD2, TMEM113, WDR82A |
|
|
87
|
|
|
Wnt family member 5B |
- |
|
|
88
|
|
|
WD repeat domain 73 |
GAMOS, GAMOS1, HSPC264 |
Aqueductal stenosis, Brain atrophy, Camos syndrome, Cataract, Cerebellar atrophy, Cerebral atrophy, Congenital camptodactyly, Congenital clubfoot, Congenital epicanthus, Developmental delay, Dwarfism, Dysarthria, Galloway-mowat syndrome, Glomerulosclerosis, Hemiplegia/hemiparesis, Hiatal hernia, High palate, Hypoalbuminemia, Hypopigmentation disorder, Hypoplasia of corpus callosum, Hypoplasia of iris, Impaired cognition, Kidney disease, Macrostomia, Macrotia, Mental retardation, Mesangial sclerosis, Microcephaly, Micrognathism, Microphthalmos, Motor delay, Nephrotic syndrome, Nystagmus, Optic atrophy, Pachygyria, Ptosis, Renal insufficiency, Spinocerebellar ataxia, StrabismusView all (24 more) |
|
89
|
|
|
WASP family member 1 |
NEDALVS, SCAR1, WAVE, WAVE-1, WAVE1 |
|
|
90
|
|
|
WASP like actin nucleation promoting factor |
N-WASP, NWASP, WASPB |
|
