cranioectodermal dysplasia 2

Term ID

DOID:0080804

Synonyms

Definition

A cranioectodermal dysplasia that has_material_basis_in compound heterozygous mutation in the WDR35 gene on chromosome 2p24. https://pubmed.ncbi.nlm.nih.gov/21378380/

References

• OMIM:613610

Ontology

Human Disease   ( DOID:0080804 )