Search Ontology:
Human Disease

holoprosencephaly 11

Term ID
DOID:0110877
Synonyms
  • HPE11
Definition
A holoprosencephaly that has_material_basis_in heterozygous mutation in the CDON gene on chromosome 11q24. https://www.ncbi.nlm.nih.gov/pubmed/21802063
References
Ontology
Human Disease   ( DOID:0110877 )
Relationships
is a type of
Other Pages
Alliance (1)
Genes Involved
Zebrafish Models
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