OBO ID: DOID:0110877 |
Term Name: | holoprosencephaly 11 | Search Ontology: | |
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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 | ||
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Ontology: | Human Disease ( DOID:0110877 ) |
OTHER holoprosencephaly 11 PAGES
ZEBRAFISH MODELS
No data available
PHENOTYPE
No data available
CITATIONS: None
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