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DO Term : chromosome Xp21 deletion syndrome [DOID:0060427] Disease Ontology

Namespace

disease_ontology

Obsolete

false

description

A chromosomal deletion syndrome that has_material_basis_in deletion of the chromosome Xp21 region.

synonyms:
ORDO:261476,
300679,
monosomy Xp21,
OMIM:300679,
ICD10CM:Q99.8,
Xp21 microdeletion syndrome,
complex glycerol kinase deficiency

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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