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Summary Literature (2)
DOID:11193 - syndactyly


Disease Ontology Definition:A synostosis that results_in the fusion of two or more digits.

Synonyms: chromosome 2q35 duplication syndrome, symphalangism, symphalangy, webbing of digits

Xenbase Genes : hoxd13, fgf16, gja1, lmbr1, fbln1

Mondo Disease Ontology (on Monarch Initiative):
MONDO:0021002 - syndactyly (disease)

OMIM:
OMIM:186100 - SYNDACTYLY, TYPE III; SDTY3
OMIM:186200 - SYNDACTYLY, TYPE IV; SDTY4
OMIM:186300 - SYNDACTYLY, TYPE V; SDTY5

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

Ontology Viewers: Disease Ontology, EMBL-EBI, OLSVis tree view, Ontobee
Parent(s): chromosomal duplication syndrome (is_a), synostosis (is_a)