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DO Term : Meier-Gorlin syndrome 8 [DOID:0080255] Disease Ontology

Namespace  disease_ontology Obsolete  false
description  A Meier-Gorlin syndrome that has_material_basis_in compound heterozygous mutation in the MCM5 gene on chromosome 22q12.
  • synonyms:
  • 617564,
  • OMIM:617564
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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