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Metadata
ID DOID:0110877
Name holoprosencephaly 11
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
Xrefs

OMIM:614226

Synonyms

HPE11 [EXACT]

Parent Relationships

is_a holoprosencephaly

is_a autosomal dominant disease

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