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Echinobase
Summary Literature (0)
DOID:0080512 - Meier-Gorlin syndrome 1

Disease Ontology Definition:A Meier-Gorlin syndrome that has_material_basis_in homozygous or compound heterozygous mutation in the ORC1 gene on chromosome 1p32.

Synonyms:

Echinobase Genes : orc1


OMIM:
MIM:224690 - meier-gorlin syndrome 1; mgors1

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

Ontology Viewers: Disease Ontology, EMBL-EBI, OLSVis tree view, Ontobee
Parent(s): Meier-Gorlin syndrome (is_a), autosomal recessive disease (is_a)