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DOID:0110975 - brachydactyly type B2
Disease Ontology Definition:A brachydactyly characterized by hypoplasia/aplasia of distal phalanges, distal symphalangism, fusion of carpal/tarsal bones, and partial cutaneous syndactyly that has_material_basis_in mutations in the NOG gene on chromosome 17q22.
Synonyms: BDB2
Xenbase Genes
:
nog
| MONDO:0012658 - brachydactyly type B2 |
| MIM:611377 - BRACHYDACTYLY, TYPE B2; BDB2 |
Other Model Organisms: Alliance, MGI, ZFIN, FlyBase, WormBase, RGD
Ontology Viewers: Disease Ontology, EMBL-EBI, OLSVis tree view
Parent(s):
brachydactyly (is_a)