brachydactyly type B2

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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 Genes associated with this Disease Ontology entry or its descendents or its corresponding OMIM entries

Genes associated with this Disease Ontology entry or its descendents or its corresponding OMIM entries

: nog

Mondo Disease Ontology (on Monarch Initiative):

MONDO:0012658 - brachydactyly type B2

MONDO:0012658 - brachydactyly type B2

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

Ontology Viewers: Disease Ontology, EMBL-EBI, OLSVis tree view, Ontobee

Parent(s): brachydactyly (is_a)