Search Ontology:
Human Disease

holoprosencephaly 2

Term ID
DOID:0110872
Synonyms
  • HPE2
Definition
A holoprosencephaly that has_material_basis_in mutation in the homeobox-containing SIX3 gene on chromosome 2p21. https://www.ncbi.nlm.nih.gov/pubmed/10369266
References
Ontology
Human Disease   ( DOID:0110872 )
Relationships
is a type of
Other Pages
Alliance (1)
Genes Involved
Zebrafish Models
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