OBO ID: DOID:0080806
Term Name: cranioectodermal dysplasia 4 Search Ontology:
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:
Ontology: Human Disease   ( DOID:0080806 )
Relationships
is a type of:
OTHER cranioectodermal dysplasia 4 PAGES
GENES INVOLVED
Human Gene Zebrafish Ortholog OMIM Term OMIM Phenotype ID
WDR19 Cranioectodermal dysplasia 4 614378
ZEBRAFISH MODELS No data available
PHENOTYPE No data available

CITATIONS: None
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