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Summary Literature (0)
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 Disease Ontology (on Monarch Initiative):
MONDO:0012658 - brachydactyly type B2


Other Model Organisms: Alliance, MGI, ZFIN, FlyBase, WormBase, RGD

Ontology Viewers: Disease Ontology, EMBL-EBI, OLSVis tree view, Ontobee
Parent(s): brachydactyly (is_a)