syndactyly type 1

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Summary

Literature (0)

DOID:0111816 - syndactyly type 1

Disease Ontology Definition:A syndactyly characterized by complete or partial webbing between the third and fourth fingers and/or the second and third toes that has_material_basis_in heterozygous duplication of a region of chromosome 2q34-q36.

Synonyms: SDTY1, chromosome 2q35 duplication syndrome, syndactyly, type 1, with or without craniosynostosis,

Echinobase 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

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

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

Parent(s): autosomal dominant disease (is_a), chromosomal duplication syndrome (is_a), syndactyly (is_a)