OBO ID: DOID:0110877
Term Name: holoprosencephaly 11 Search Ontology:
Synonyms:
  • HPE11
Definition: A holoprosencephaly that has_material_basis_in heterozygous mutation in the CDON gene on chromosome 11q24. https://www.ncbi.nlm.nih.gov/pubmed/21802063
References:
Ontology: Human Disease   ( DOID:0110877 )
OTHER holoprosencephaly 11 PAGES
GENES INVOLVED
Human Gene Zebrafish Ortholog OMIM Term OMIM Phenotype ID
CDON Holoprosencephaly 11 614226
ZEBRAFISH MODELS No data available
PHENOTYPE No data available

CITATIONS: None