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DO Term : cranioectodermal dysplasia 2 [DOID:0080804] Disease Ontology

Namespace

disease_ontology

Obsolete

false

description

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

synonyms:
OMIM:613610,
613610

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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