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DO Term : Meier-Gorlin syndrome 3 [DOID:0080514] Disease Ontology

Namespace

disease_ontology

Obsolete

false

description

A Meier-Gorlin syndrome that has_material_basis_in homozygous or compound heterozygous mutation in the ORC6 gene on chromosome 16q11.

synonyms:
OMIM:613803,
613803

Disease

Diseases --> Human genes

Diseases --> Mouse genes

Diseases --> Mouse models

Ontology

Ontology Term --> All ancestors

Ontology Term --> All descendants

Ontology Term --> Direct children

Ontology Term --> Direct parents

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