cranioectodermal dysplasia 2

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Echinobase

Summary

Literature (0)

DOID:0080804 - cranioectodermal dysplasia 2

Disease Ontology Definition:A cranioectodermal dysplasia that has_material_basis_in compound heterozygous mutation in the WDR35 gene on chromosome 2p24.

Synonyms:

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

: wdr35

MIM:

MIM:613610 - cranioectodermal dysplasia 2; ced2

MIM:613610 - cranioectodermal dysplasia 2; ced2

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

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

Parent(s): cranioectodermal dysplasia (is_a)