synpolydactyly
syndactyly characterized by an increased number of digits; often a result of a mutation in the HOX D13 gene
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synpolydactyly
Summary
synpolydactyly is a developmental defect during embryogenesis[1].
Key Facts
- synpolydactyly's instance of is recorded as developmental defect during embryogenesis[2].
- synpolydactyly's instance of is recorded as rare disease[3].
- synpolydactyly's instance of is recorded as class of disease[4].
- synpolydactyly is a type of syndactyly[5].
- synpolydactyly is a type of polydactyly[6].
- synpolydactyly is a type of dysostosis of genetic origin with limb anomaly as a major feature[7].
- synpolydactyly's NCI Thesaurus ID is recorded as C75005[8].
- synpolydactyly's NCI Thesaurus ID is recorded as C75003[9].
- synpolydactyly's genetic association is recorded as FBLN1[10].
- synpolydactyly's genetic association is recorded as HOXD13[11].
- synpolydactyly's exact match is recorded as http://purl.obolibrary.org/obo/DOID_0060242[12].
- synpolydactyly's exact match is recorded as http://identifiers.org/doid/DOID:0060242[13].
- synpolydactyly's exact match is recorded as http://www.orpha.net/ORDO/Orphanet_295195[14].
- synpolydactyly's on focus list of Wikimedia project is recorded as WikiProject Medicine[15].