|
271
|
|
|
Intraflagellar transport 52 |
C20orf9, CGI-53, NGD2, NGD5 |
Asphyxiating thoracic dystrophy, Brachydactyly, Camptodactyly of fingers, Congenital epicanthus, Congenital pectus excavatum, Cranioectodermal dysplasia, Craniosynostosis, Dolichocephaly, Dwarfism, Frontal bossing, Gastrointestinal stromal tumor, Hyperopia, Hypodontia, Hypoplasia of corpus callosum, Majewski syndrome, Microdontia, Motor delay, Myopia, Nystagmus, Osteoporosis, Polydactyly, Rhizomelia, Short rib-polydactyly syndrome, Short-rib thoracic dysplasia with or without polydactyly, Syndactyly of fingers, TaurodontismView all (11 more) |
|
272
|
|
|
Immediate early response 3 interacting protein 1 |
HSPC039, MEDS, PRO2309 |
Developmental delay, Diabetes mellitus, Epilepsy, High palate, Hypoplasia of corpus callosum, Mental retardation, Microcephaly, Microcephaly, epilepsy, and diabetes syndrome, Myoclonic seizures, Hypotonia, Microcephaly-epilepsy-permanent diabetes syndrome, Ptosis |
|
273
|
|
|
Interleukin 1 receptor associated kinase 4 |
IMD67, IPD1, IRAK-4, NY-REN-64, REN64 |
Anorexia, Anoxic-ischemic encephalopathy, Cerebral hypoxia-ischemia, Hypoxic-ischemic encephalopathy, Immunodeficiency, Immunologic deficiency syndromes, Irak4 deficiency, Ischemic encephalopathy, Lupus erythematosus, Neutropenia, Nonbacterial verrucal endocardiosis, Prostatic neoplasms, Prostate cancer |
|
274
|
|
|
Inhibitor of growth family member 4 |
my036, p29ING4 |
|
|
275
|
|
|
Importin 11 |
RanBP11 |
|
|
276
|
|
|
IGF2 antisense RNA |
IGF2-AS1, IGF2AS, PEG8 |
Ankylosing spondylitis, Arthritis, Autoimmune diseases, Autoimmune thyroiditis, Celiac disease, Common variable immunodeficiency, Crohn disease, Diabetes mellitus, Lupus erythematosus, Psoriasis, Ulcerative colitis |
|
277
|
|
|
Inositol hexakisphosphate kinase 2 |
IHPK2, InsP6K2, PIUS |
|
|
278
|
|
|
Inositol-3-phosphate synthase 1 |
INO1, INOS, IPS, IPS 1, IPS-1 |
|
|
279
|
|
|
Interleukin 23 subunit alpha |
IL-23, IL-23A, IL23P19, P19, SGRF |
|
|
280
|
|
|
Inositol polyphosphate-5-phosphatase K |
MDCCAID, PPS, SKIP |
Avascular necrosis of the capital femoral epiphysis, Brachydactyly, Breast cancer, Cataract, Cerebellar hypoplasia, Congenital pectus carinatum, Developmental delay, Dwarfism, Dysarthria, Dyskinetic syndrome, Hypogonadism, Legg-calve-perthes disease, Marinesco-sjogren syndrome, Mental retardation, Microcephaly, Motor delay, Muscular dystrophy, Congenital muscular dystrophy, with cataracts and intellectual disability, Myopathy, Nervous system diseases, Nystagmus, Optic atrophy, Scoliosis, Specific learning disorder, StrabismusView all (10 more) |
