OBO ID: DOID:0110876
Term Name: holoprosencephaly 7 Search Ontology:
Synonyms:
  • HPE7
Definition: A holoprosencephaly that has_material_basis_in heterozygous mutation in the PTCH1 gene on chromosome 9q22. https://www.ncbi.nlm.nih.gov/pubmed/11941477
References:
Ontology: Human Disease   ( DOID:0110876 )
Relationships
is a type of:
OTHER holoprosencephaly 7 PAGES
GENES INVOLVED
Human Gene Zebrafish Ortholog OMIM Term OMIM Phenotype ID
PTCH1 Holoprosencephaly 7 610828
ZEBRAFISH MODELS No data available
PHENOTYPE No data available

CITATIONS: None
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