OBO ID: DOID:0080346
Term Name: blepharocheilodontic syndrome 2 Search Ontology:
Synonyms:
Definition: A blepharocheilodontic syndrome that has_material_basis_in heterozygous mutation in the CTNND1 gene on chromosome 11q12. https://www.ncbi.nlm.nih.gov/pubmed/28301459
References:
Ontology: Human Disease   ( DOID:0080346 )
Relationships
is a type of:
OTHER blepharocheilodontic syndrome 2 PAGES
GENES INVOLVED
Human Gene Zebrafish Ortholog OMIM Term OMIM Phenotype ID
CTNND1 Blepharocheilodontic syndrome 2 617681
ZEBRAFISH MODELS No data available
PHENOTYPE No data available

CITATIONS: None
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