OBO ID: DOID:0110872
Term Name: holoprosencephaly 2 Search Ontology:
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 holoprosencephaly 2 PAGES
GENES INVOLVED
Human Gene Zebrafish Ortholog OMIM Term OMIM Phenotype ID
SIX3 Holoprosencephaly 2 157170
ZEBRAFISH MODELS No data available
PHENOTYPE No data available

CITATIONS: None
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