|
171
|
|
|
R-spondin 4 |
C20orf182, CRISTIN4 |
|
|
172
|
|
|
Radial spoke head component 4A |
CILD11, RSHL3, RSPH6B, dJ412I7.1 |
Asthenozoospermia, Asthma, Bronchiectasis, Ciliary dyskinesia, Asplenia, Congenital pectus excavatum, Corneal dystrophy, Dwarfism, Bronchitis, Hearing loss, Hydrocephalus, Lung diseases, Nasal polyposis, Otitis media, Rhinitis, Scoliosis, Sinusitis, Situs inversusView all (3 more) |
|
173
|
|
|
RAF1 pseudogene 1 |
- |
|
|
174
|
|
|
Recombination signal binding protein for immunoglobulin kappa J region |
AOS3, CBF-1, CBF1, IGKJRB, IGKJRB1, KBF2, RBP-J, RBP-J kappa, RBP-JK, RBPJK, RBPSUH, SUH, csl |
Acquired porencephaly, Adams-oliver syndrome, Alopecia, Aplasia cutis congenita, Brachydactyly, Cataract, Cirrhosis, Congenital arteriovenous malformation, Congenital atresia of pulmonary artery, Congenital cerebral hernia, Congenital hepatic fibrosis, Cutis marmorata, Diabetes mellitus, Dysmorphic features, Endometrioma, Endometriosis, Esophageal varix, Hydrocephalus, Leukopenia, Mental retardation, Microcephaly, Microphthalmos, Multiple congenital anomalies, Multiple sclerosis, Periventricular leukomalacia, Porencephalic cyst, Portal hypertension, Pulmonary arterial hypertension, Rheumatoid arthritis, Strabismus, Syndactyly of fingers, Syndactyly of the toes, Talipes, Tetralogy of fallotView all (19 more) |
|
175
|
|
|
Retinoic acid early transcript 1M (pseudogene) |
- |
|
|
176
|
|
|
Refilin B |
CFM1, FAM101B |
|
|
177
|
|
|
Ribosomal protein S10 pseudogene 7 |
RPS10_2_147, lnc-MCEI |
|
|
178
|
|
|
Ras homolog family member A |
ARH12, ARHA, EDFAOB, RHO12, RHOH12 |
Alopecia, Alopecia, male pattern, Anaplastic carcinoma, Androgenetic alopecia, Angioimmunoblastic t-cell lymphoma, Aplasia cutis congenita, Urinary bladder cancer, Bladder neoplasm, Mammary neoplasms, Burkitt`s lymphoma, Carcinoma, Carcinoma of the head and neck, Colorectal neoplasms, Congenital diaphragmatic hernia, Congenital ectodermal dysplasia of face, Posterolateral diaphragmatic hernia, Morgagni diaphragmatic hernia, Coronary artery disease, Crohn disease, Ectodermal dysplasia, Esophageal carcinoma, Gastric cancer, Gastrointestinal stromal tumor, Granulomatous slack skin, Hidrotic ectodermal dysplasia, Hypohidrotic ectodermal dysplasia, Hypopigmentation disorder, Leukoencephalopathy, Leukoencephalopathy with vanishing white matter, Lung adenocarcinoma, Lymphoma, Neurocutaneous syndromes, Pseudopelade, Stomach neoplasms, T-cell lymphoma, Tooth diseasesView all (21 more) |
|
179
|
|
|
RAS like family 11 member A |
- |
|
|
180
|
|
|
Ras homolog family member B |
ARH6, ARHB, MST081, MSTP081, RHOH6 |
|
