OBO ID: DOID:0080345
Term Name: blepharocheilodontic syndrome 1 Search Ontology:
Synonyms:
Definition: A blepharocheilodontic syndrome that has_material_basis_in heterozygous mutation in the CDH1 gene on chromosome 16q22. https://www.ncbi.nlm.nih.gov/pubmed/28301459
References:
Ontology: Human Disease   ( DOID:0080345 )
Relationships
is a type of:
OTHER blepharocheilodontic syndrome 1 PAGES
GENES INVOLVED
Human Gene Zebrafish Ortholog OMIM Term OMIM Phenotype ID
CDH1 Blepharocheilodontic syndrome 1 119580
ZEBRAFISH MODELS No data available
PHENOTYPE No data available

CITATIONS: None
Your Input Welcome
We welcome your input and comments. Please use this form to recommend updates to the information in ZFIN. We appreciate as much detail as possible and references as appropriate. We will review your comments promptly.
Please check the highlighted fields and try again.
Thank you for submitting comments. Your input has been emailed to ZFIN curators who may contact you if additional information is required.
Oops. Something went wrong. Please try again later.