Search Ontology:
Human Disease

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
Ontology
Human Disease   ( DOID:0080804 )
Relationships
is a type of
Other Pages
Alliance (1)
Genes Involved
Zebrafish Models
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