Click here to close Hello! We notice that you are using Internet Explorer, which is not supported by Xenbase and may cause the site to display incorrectly. We suggest using a current version of Chrome, FireFox, or Safari.
Summary Literature (0)
DOID:0110965 - brachydactyly type A2


Disease Ontology Definition:A brachydactyly characterized by autosomal dominant inheritance of malformations of the middle phalanx of the index finger and anomalies of the second toe that has_material_basis_in heterozygous mutation in the BMPR1B gene on chromosome 4q or in the GDF5 gene on chromosome 20q11 or heterozygous duplication in a regulatory element of BMP2 on chromosome 20p12.

Synonyms: BDA2, Mohr-Wriedt type brachydactyly, brachymesophalangy II

In OMIM:
OMIM:112600 - BRACHYDACTYLY, TYPE A2; BDA2

In Mondo Disease Ontology:
MONDO:0007216 - brachydactyly type A2

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

Xenbase Genes : gdf5, bmp2, bmpr1b

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