|
71
|
|
|
Wnt family member 7A |
SANTOS, Wnt-7a |
Al awadi syndrome, Amyotrophic lateral sclerosis, Elbow ankylosis, Anonychia, Clinodactyly, Congenital clubfoot, Developmental dysplasia of the hip, Congenital epicanthus, Congenital hypoplasia of penis, Congenital hypoplasia of radius, Congenital meningocele, Congenital pectus carinatum, Cryptorchidism, Dwarfism, Ectrodactyly, Elbow flexion contracture, Female urogenital diseases, Fuhrmann syndrome, Genitourinary cancer, Genitourinary neoplasms, High palate, Hydrops fetalis, Hypoplasia of nipple, Hypospadias, Imperforate anus, Lateral sclerosis, Micrognathism, Micromelia, Nail diseases, Nail dysplasia, Ovarian neoplasm, Ovarian cancer, Phocomelia, Polydactyly, Ramer ladda syndrome, Syndactyly of the toes, Talipes, Postaxial hand polydactylyView all (23 more) |
|
72
|
|
|
Wnt family member 7B |
- |
|
|
73
|
|
|
Wnt family member 8A |
WNT8D |
|
|
74
|
|
|
Wnt family member 8B |
- |
|
|
75
|
|
|
Wnt family member 10B |
SHFM6, STHAG8, WNT-12 |
Aniridia, Breast cancer, Breast carcinoma, Ectrodactyly, Hearing loss, Hypodontia, Hypoplasia of the maxilla, Isolated split hand-split foot malformation, Mammary neoplasms, Marfan syndrome, Microdontia, Micrognathism, Oligodactyly, Oligodontia, Polydactyly, Prostate cancer, Prostatic neoplasms, Split hand foot deformity, Split-hand-foot malformation, Syndactyly of fingers, Syndactyly of the toes, Tooth agenesisView all (7 more) |
|
76
|
|
|
Wnt family member 11 |
HWNT11 |
|
|
77
|
|
|
Wnt family member 2B |
WNT13 |
|
|
78
|
|
|
WRN RecQ like helicase |
RECQ3, RECQL2, RECQL3 |
Acral lentiginous malignant melanoma, Arteriosclerosis, Atherosclerosis, Breast carcinoma, Carcinoma, Cardiovascular diseases, Cataract, Chondrocalcinosis, Chromosome instability syndromes, Colorectal cancer, Congestive heart failure, Diabetes mellitus, Dna repair-deficiency disorders, Dwarfism, Gastrointestinal carcinoma, Hyperkeratosis, Hypertension, Hypogonadism, Intestinal neoplasms, Kidney neoplasm, Laryngomalacia, Leukemia, Lipoatrophy, Lipodystrophy, Lung neoplasms, Malignant neoplasm, Medulloblastoma, Meningioma, Mouth neoplasms, Myocardial infarction, Osteoporosis, Osteosarcoma, Osteosclerosis, Ovarian neoplasm, Premature aging, Sarcoma, Scleroderma, Secondary physiologic amenorrhea, Subcutaneous calcification, Thyroid carcinoma, Vertical talus, Werner syndromeView all (27 more) |
|
79
|
|
|
WT1 transcription factor |
AWT1, GUD, NPHS4, WAGR, WIT-2, WT-1, WT33 |
11p deletion syndrome, 46, xy complete gonadal dysgenesis, 46, xy partial gonadal dysgenesis, Ambiguous genitalia, Anemia, Aniridia, Aortic coarctation, Aortic valve sclerosis, Atresia of vagina, Atrial septal defect, Azoospermia, B-cell lymphoma, Breast cancer, Breast carcinoma, Bright disease, Bronchopulmonary disease, Cataract, Central nervous system neoplasms, Colonic neoplasms, Congenital diaphragmatic hernia, Congenital hypoplasia of penis, Contiguous gene syndrome, Cryptorchidism, Denys-drash syndrome, Desmoplastic tumor, Disorder of eye, Dwarfism, Frasier syndrome, Genetic steroid-resistant nephrotic syndrome, Giant cell glioblastoma, Glaucoma, Glioblastoma, Glomerulonephritis, Glomerulosclerosis, Gonadal dysgenesis, Gonadal dysgenesis with female appearance, male, Gonadoblastoma, Gonadotropin-resistant ovary syndrome, Gynecomastia, Horseshoe kidney, Hydrometrocolpos, Hypertension, Hypertrophy of clitoris, Hypogonadism, Hypogonadotropic hypogonadism, Hypoplasia of corpus callosum, Hypoplasia of the optic nerve, Hypoplasia of vagina, Hypoplastic left heart syndrome, Hypospadias, Ileus, Kidney disease, Leukemia, Liver neoplasms, Lung cancer, Lung neoplasms, Male pseudohermaphroditism, Malignant mesothelioma, Mammary neoplasms, Marfan syndrome, Meacham syndrome, Mediastinal lymphadenopathy, Mental retardation, Mesangial sclerosis, Mesothelioma, Microcephaly, Micrognathism, Morgagni diaphragmatic hernia, Myeloid leukemia, Nephritis, Nephroblastoma, Nephrosis, congenital, Nephrotic syndrome, Neurilemmoma, Nystagmus, Obesity, Osteoporosis, Osteosarcoma, Ovarian failure, Ovarian gonadoblastoma, Ovarian neoplasm, Pancreatic cancer, Pancreatic neoplasm, Patent ductus arteriosus, Penis agenesis, Peritoneal carcinomatosis, Peritoneal neoplasms, Physiologic amenorrhea, Polycystic ovary syndrome, Polymicrogyria, Posterolateral diaphragmatic hernia, Premature ovarian failure, Promyelocytic leukemia, Ptosis, Pulmonary venous return anomaly, Renal glomerular disease, Renal insufficiency, Sarcoma, Schwannomatosis, Scoliosis, Situs inversus, Streak ovary, Swyer syndrome, Testicular dysgenesis, Testicular gonadoblastoma, Testicular neoplasms, Testicular regression syndrome, Tetralogy of fallot, Transposition of great vessels, True hermaphroditism, Ventricular septal defect, Wagner syndrome, Wagr syndrome, Wilms tumorView all (99 more) |
|
80
|
|
|
WD repeat domain 77 |
HKMT1069, MEP-50, MEP50, Nbla10071, p44, p44/Mep50 |
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