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Summary Literature (0)
DOID:0111817 - syndactyly type 3

Disease Ontology Definition:A syndactyly characterized by complete and bilateral syndactyly between the 4th and 5th fingers that has_material_basis_in heterozygous mutation in the GJA1 gene on chromosome 6q22.31.

Synonyms: ringand little finger syndactyly, SDTY3, syndactyly of fingers 4 and 5, syndactyly, type III

Xenbase Genes : gja1


MIM:
MIM:186100 - SYNDACTYLY, TYPE III; SDTY3

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

Ontology Viewers: Disease Ontology, EMBL-EBI, OLSVis tree view, Ontobee
Parent(s): autosomal dominant disease (is_a), syndactyly (is_a)