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DOID:0050690 - brachyolmia
Disease Ontology Definition:An osteochondrodysplasia characterized by generalized platyspondyly without significant long bone abnormalities and short stature.
Synonyms: brachyrachia
Xenbase Genes
:
trpv4
| MONDO:0015262 - brachyolmia |
| MIM:113500 - BRACHYOLMIA TYPE 3; BCYM3 |
| MIM:271530 - BRACHYOLMIA TYPE 1, HOBAEK TYPE; BCYM1A |
| MIM:271630 - BRACHYOLMIA TYPE 1, TOLEDO TYPE; BCYM1B |
| MIM:613678 - BRACHYOLMIA TYPE 2; BCYM2 |
Other Model Organisms: Alliance, MGI, ZFIN, FlyBase, WormBase, RGD
Ontology Viewers: Disease Ontology, EMBL-EBI, OLSVis tree view, Ontobee
Parent(s):
osteochondrodysplasia (is_a)