OBO ID: DOID:0080805
Term Name: cranioectodermal dysplasia 3 Search Ontology:
Synonyms:
Definition: A cranioectodermal dysplasia that has_material_basis_in homozygous mutation in the IFT43 gene on chromosome 14q24. https://pubmed.ncbi.nlm.nih.gov/21378380/
References:
Ontology: Human Disease   ( DOID:0080805 )
Relationships
is a type of:
OTHER cranioectodermal dysplasia 3 PAGES
GENES INVOLVED
Human Gene Zebrafish Ortholog OMIM Term OMIM Phenotype ID
IFT43 ?Cranioectodermal dysplasia 3 614099
ZEBRAFISH MODELS No data available
PHENOTYPE No data available

CITATIONS: None
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