OBO ID: DOID:0110873
Term Name: holoprosencephaly 9 Search Ontology:
Synonyms:
  • holoprosencephaly with microphthalmia and first branchial arch anomalies
  • HPE9
  • pituitary anomalies with holoprosencephaly-like features
Definition: A holoprosencephaly that has_material_basis_in heterozygous mutation in the GLI2 gene on chromosome 2q14. https://www.ncbi.nlm.nih.gov/pubmed/14581620
References:
Ontology: Human Disease   ( DOID:0110873 )
OTHER holoprosencephaly 9 PAGES
GENES INVOLVED
Human Gene Zebrafish Ortholog OMIM Term OMIM Phenotype ID
GLI2 Holoprosencephaly 9 610829
ZEBRAFISH MODELS No data available
PHENOTYPE No data available

CITATIONS: None