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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

In OMIM:
OMIM:611377 - BRACHYDACTYLY, TYPE B2; BDB2

In Mondo Disease Ontology:
MONDO:0012658 - brachydactyly type B2

Human Disease Resources: Disease Ontology, EMBL-EBI, OLSVis tree view, Ontobee

Xenbase Genes : nog

Other Model Organisms: AGR, MGI, ZFIN, FlyBase, WormBase, RGD
Parent(s): brachydactyly (is_a)