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Summary Literature (0)
DOID:0111603 - distal arthrogryposis type 7

Disease Ontology Definition:A distal arthrogryposis characterized by inability to open the mouth fully and pseudocamptodactyly that has_material_basis_in heterozygous mutation in the MYH8 gene on chromosome 17p13.1.

Synonyms: DA7, Dutch-Kentucky syndrome, Hecht-Beals syndrome, Hecht syndrome, mouth, inability to completely open, and short finger-flexor tendons, trismus-pseudocamptodactyly syndrome

Xenbase Genes : myh8



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), distal arthrogryposis (is_a)