holoprosencephaly 1

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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,

Xenbase Genes Genes associated with this Disease Ontology entry or its descendents or its corresponding OMIM entries

Genes associated with this Disease Ontology entry or its descendents or its corresponding OMIM entries

: foxh1.2, foxh1

Mondo Disease Ontology (on Monarch Initiative):

MONDO:0009349 - holoprosencephaly 1

MONDO:0009349 - holoprosencephaly 1

OMIM:

OMIM:236100 - HOLOPROSENCEPHALY 1; HPE1

OMIM:236100 - HOLOPROSENCEPHALY 1; HPE1

Other Model Organisms: AGR, MGI, ZFIN, FlyBase, WormBase, RGD

Ontology Viewers: Disease Ontology, EMBL-EBI, OLSVis tree view, Ontobee

Parent(s): holoprosencephaly (is_a)