Search Ontology:
Human Disease

holoprosencephaly 5

Term ID
DOID:0110878
Synonyms
  • HPE5
Definition
A holoprosencephaly that has_material_basis_in heterozygous mutation in the ZIC2 gene on chromosome 13q32. https://www.ncbi.nlm.nih.gov/pubmed/9771712
References
Ontology
Human Disease   ( DOID:0110878 )
Relationships
is a type of
Other Pages
Alliance (1)
Genes Involved
Zebrafish Models
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