Search Ontology:
Human Disease

holoprosencephaly 7

Term ID
DOID:0110876
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
Other Pages
Alliance (1)
Genes Involved
Zebrafish Models
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