Search Ontology:
Human Disease

blepharocheilodontic syndrome 2

Term ID
DOID:0080346
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 Pages
Alliance (1)
Genes Involved
Zebrafish Models
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