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Summary Literature (0)
DOID:0111818 - syndactyly type 4

Disease Ontology Definition:A syndactyly characterized by complete bilateral syndactyly involving all digits 1 to 5 that has_material_basis_in heterozygous mutation of a SHH regulatory element in intron 5 of the LMBR1 gene on chromosome 7q36.3.

Synonyms: Haas type syndactyly, polysyndactyly, Haas type, SDTY4

Xenbase Genes : lmbr1


MIM:
MIM:186200 - SYNDACTYLY, TYPE IV; SDTY4

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)