chromosome Xp21 deletion syndrome

Term ID

DOID:0060427

Synonyms

• complex glycerol kinase deficiency
• monosomy Xp21
• Xp21 microdeletion syndrome

Definition

A chromosomal deletion syndrome that has_material_basis_in deletion of the chromosome Xp21 region. https://pubmed.ncbi.nlm.nih.gov/17089405/

References

• ICD10CM:Q99.8
• OMIM:300679
• ORDO:261476

Ontology

Human Disease   ( DOID:0060427 )