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DO Term : ring chromosome syndrome [DOID:0070620] Disease Ontology

Namespace

disease_ontology

Obsolete

false

description

A chromosomal disease that has_material_basis_in chromosome fusion into a ring or ring-like structure. Ring chromosome syndrome phenotypes are inherently variable.

synonyms:
MESH:D012303,
ring chromosome,
ring syndrome,
ORDO:363203,
UMLS_CUI:C0035639,
RC,
ICD10CM:Q93.2

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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