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Disease Ontology Browser
holoprosencephaly 9 (DOID:0110873)
Synonyms: holoprosencephaly with microphthalmia and first branchial arch anomalies; HPE9; pituitary anomalies with holoprosencephaly-like features
Alt IDs: OMIM:610829
Definition: A holoprosencephaly that has_material_basis_in heterozygous mutation in the GLI2 gene on chromosome 2q14.


Contributing Projects:
Mouse Genome Database (MGD), Gene Expression Database (GXD), Mouse Tumor Biology (MTB), Gene Ontology (GO), MouseCyc
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last database update
05/16/2017
MGI 6.09
The Jackson Laboratory