cranioectodermal dysplasia 4

Term ID

DOID:0080806

Synonyms

Definition

A cranioectodermal dysplasia that has_material_basis_in compound heterozygous mutation in the WDR19 gene on chromosome 4p14. https://pubmed.ncbi.nlm.nih.gov/21378380/

References

• OMIM:614378

Ontology

Human Disease   ( DOID:0080806 )