Search Ontology:
Human Disease

craniosynostosis 3

Term ID
DOID:0061011
Synonyms
  • CRS3
Definition
A craniosynostosis that has_material_basis_in heterozygous mutation in the TCF12 gene on chromosome 15q21. https://pubmed.ncbi.nlm.nih.gov/23438589/
References
Ontology
Human Disease   ( DOID:0061011 )
Relationships
is a type of
Other Pages
Genes Involved
Zebrafish Models
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