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Disease Ontology Browser
synpolydactyly (DOID:0060242)
Alliance: disease page
Synonyms: syndactyly type 2
Alt IDs: OMIM:186000, OMIM:608180, OMIM:610234, MESH:C538153, NCI:C75003, NCI:C75005, ORDO:295195, UMLS_CUI:C2699746
Definition: A syndactyly characterized by an increased number of digits; often a result of a mutation in the HOX D13 gene.

Disease References using Mouse Models (4)

Contributing Projects:
Mouse Genome Database (MGD), Gene Expression Database (GXD), Mouse Models of Human Cancer database (MMHCdb) (formerly Mouse Tumor Biology (MTB), Gene Ontology (GO)
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last database update
01/21/2020
MGI 6.14
The Jackson Laboratory