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DO Term : syndactyly type 3 [DOID:0111817] Disease Ontology

Namespace

disease_ontology

Obsolete

false

description

A syndactyly characterized by complete and bilateral syndactyly between the 4th and 5th fingers that has_material_basis_in heterozygous mutation in the GJA1 gene on chromosome 6q22.31.

synonyms:
ORDO:93404,
ringand little finger syndactyly,
OMIM:186100,
SNOMEDCT_US_2023_03_01:715725001,
UMLS_CUI:C1861366,
syndactyly, type III,
MESH:C538154,
syndactyly of fingers 4 and 5,
GARD:5088,
186100,
SDTY3

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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