OBO ID: DOID:0110875
Term Name: holoprosencephaly 3 Search Ontology:
Synonyms:
  • HLP3
  • HPE3
Definition: A holoprosencephaly that has_material_basis_in heterozygous mutation in the SHH gene on chromosome 7q36. https://www.ncbi.nlm.nih.gov/pubmed/8896572
References:
Ontology: Human Disease   ( DOID:0110875 )
Relationships
is a type of:
OTHER holoprosencephaly 3 PAGES
GENES INVOLVED
Human Gene Zebrafish Ortholog OMIM Term OMIM Phenotype ID
SHH Holoprosencephaly 3 142945
ZEBRAFISH MODELS No data available
PHENOTYPE No data available

CITATIONS: None
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