|
41
|
|
|
WD repeat domain 74 |
Nsa1 |
|
|
42
|
|
|
WW domain binding protein 1 like |
C10orf26, OPA1L, OPAL1 |
|
|
43
|
|
|
WD repeat domain, phosphoinositide interacting 1 |
ATG18, ATG18A, WIPI49 |
|
|
44
|
|
|
WD repeat domain 70 |
- |
|
|
45
|
|
|
WD repeat containing antisense to TP53 |
DKCB3, TCAB1, WDR79 |
Alopecia, Anemia, Carcinoma, Cataract, Cirrhosis, Developmental delay, Diabetes mellitus, Dwarfism, Dyskeratosis congenita, Esophageal stenosis, Hypodontia, Hypoplasia of the maxilla, Leukoplakia, Liver failure, Lymphoma, Malabsorption syndrome, Nail diseases, Nail dysplasia, Nail dystrophy, Neutropenia, Osteoporosis, Palmoplantar keratoderma, Pancreatic neoplasm, Pancytopenia, Periodontitis, Scoliosis, TaurodontismView all (12 more) |
|
46
|
|
|
WD repeat domain 41 |
MSTP048 |
|
|
47
|
|
|
WD repeat domain 11 |
BRWD2, DR11, HH14, SRI1, WDR15 |
Anxiety disorder, Benign prostatic hyperplasia, Congenital camptodactyly, Breast hypoplasia, Hypoplasia of the ovary, Congenital hypoplasia of penis, Congenital sensorineural hearing loss, Cryptorchidism, Developmental delay, Diabetes insipidus, Dwarfism, Dysarthria, Erectile dysfunction, Female hypogonadism syndrome, Gynecomastia, Hearing loss, Hypoglycemia, Hypogonadotropic hypogonadism, Hypogonadotropic hypogonadism with or without anosmia, Hypopituitarism, Hypothyroidism, Ichthyosis, Kallmann syndrome, Mental depression, Mental retardation, Mirror movements, Non-obstructive azoospermia, Normosmic congenital hypogonadotropic hypogonadism, Nystagmus, Obesity, Osteochondrodysplasia, Osteopenia, Osteoporosis, Paraplegia, Penis agenesis, Physiologic amenorrhea, Pituitary stalk interruption syndrome, Ptosis, Renal agenesis, Schizophrenia, Secondary physiologic amenorrhea, Septo-optic dysplasia, Skeletal dysplasia, Testicular hypogonadismView all (29 more) |
|
48
|
|
|
WD repeat domain 12 |
YTM1 |
|
|
49
|
|
|
WD repeat domain 45B |
NEDSBAS, WDR45L, WIPI-3, WIPI3 |
|
|
50
|
|
|
WD repeat domain 93 |
C1d-87, CFAP297, FAP297 |
|
