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Summary Literature (0)
DOID:0110881 - holoprosencephaly 1


Disease Ontology Definition:A holoprosencephaly that has_material_basis_in variation in the chromosome region 21q22.3.

Synonyms: HPE1

In OMIM:
OMIM:236100 - HOLOPROSENCEPHALY 1; HPE1

In Mondo Disease Ontology:
MONDO:0009349 - holoprosencephaly 1

Human Disease Resources: Disease Ontology, EMBL-EBI, OLSVis tree view, Ontobee

Xenbase Genes : foxh1.2, foxh1

Other Model Organisms: AGR, MGI, ZFIN, FlyBase, WormBase, RGD
Parent(s): holoprosencephaly (is_a)