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DOID:0110881 - holoprosencephaly 1
Disease Ontology Definition:A holoprosencephaly that has_material_basis_in variation in the chromosome region 21q22.3.
Synonyms: HPE1,
Xenbase Genes
![Genes associated with this Disease Ontology entry or its descendents or its corresponding OMIM entries](img/icons/info1.png)
MONDO:0009349 - holoprosencephaly 1 |
Other Model Organisms: AGR, MGI, ZFIN, FlyBase, WormBase, RGD
Ontology Viewers: Disease Ontology, EMBL-EBI, OLSVis tree view, Ontobee