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Disease Ontology Browser
holoprosencephaly 7 (DOID:0110876)
Alliance: disease page
Synonyms: HPE7
Alt IDs: OMIM:610828
Definition: A holoprosencephaly that has_material_basis_in heterozygous mutation in the PTCH1 gene on chromosome 9q22.


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
10/10/2017
MGI 6.10
The Jackson Laboratory