OBO ID: DOID:0080804
Term Name: cranioectodermal dysplasia 2 Search Ontology:
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:
Ontology: Human Disease   ( DOID:0080804 )
Relationships
is a type of:
OTHER cranioectodermal dysplasia 2 PAGES
GENES INVOLVED
Human Gene Zebrafish Ortholog OMIM Term OMIM Phenotype ID
WDR35 Cranioectodermal dysplasia 2 613610
ZEBRAFISH MODELS No data available
PHENOTYPE No data available

CITATIONS: None
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