Meier-Gorlin syndrome 1

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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 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

: orc1

MIM:

MIM:224690 - meier-gorlin syndrome 1; mgors1

MIM:224690 - meier-gorlin syndrome 1; mgors1

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

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

Parent(s): autosomal recessive disease (is_a), Meier-Gorlin syndrome (is_a)