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DO Term : synpolydactyly [DOID:0060242] Disease Ontology

Namespace

disease_ontology

Obsolete

false

description

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

synonyms:
syndactyly type 2,
OMIM:186000,
OMIM:608180,
OMIM:610234,
608180,
NCI:C75003,
186000,
MESH:C538153,
SNOMEDCT_US_2023_03_01:715724002,
ORDO:295195,
UMLS_CUI:C2699746,
GARD:5087,
610234

Disease

Diseases --> Human genes

Diseases --> Mouse genes

Diseases --> Mouse models

Ontology

Ontology Term --> All ancestors

Ontology Term --> All descendants

Ontology Term --> Direct children

Ontology Term --> Direct parents

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