synpolydactyly

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Summary

Literature (0)

DOID:0060242 - synpolydactyly

Disease Ontology Definition:A syndactyly characterized by an increased number of digits; often a result of a mutation in the HOXD13 gene.

Synonyms: syndactyly type 2

Xenbase Genes Genes associated with this Disease Ontology entry or its descendents or its corresponding OMIM entries

Genes associated with this Disease Ontology entry or its descendents or its corresponding OMIM entries

: hoxd13, fbln1

Mondo Disease Ontology (on Monarch Initiative):

MONDO:0000722 - non-syndromic synpolydactyly

MONDO:0000722 - non-syndromic synpolydactyly

MIM:

MIM:186000 - SYNPOLYDACTYLY 1; SPD1
MIM:608180 - SYNPOLYDACTYLY 2; SPD2
MIM:610234 - SYNPOLYDACTYLY 3; SPD3

MIM:186000 - SYNPOLYDACTYLY 1; SPD1

MIM:608180 - SYNPOLYDACTYLY 2; SPD2

MIM:610234 - SYNPOLYDACTYLY 3; SPD3

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

Ontology Viewers: Disease Ontology, EMBL-EBI, OLSVis tree view, Ontobee

Parent(s): syndactyly (is_a)