chromosome Xp21 deletion syndrome Disease Ontology Browser

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chromosome Xp21 deletion syndrome (DOID:0060427)
Alliance: disease page
Synonyms: complex glycerol kinase deficiency; monosomy Xp21; Xp21 microdeletion syndrome
Alt IDs: OMIM:300679, ICD10CM:Q99.8, ORDO:261476
Definition: A chromosomal deletion syndrome that has_material_basis_in deletion of the chromosome Xp21 region.

Contributing Projects: Mouse Genome Database (MGD), Gene Expression Database (GXD), Mouse Models of Human Cancer database (MMHCdb) (formerly Mouse Tumor Biology (MTB)), Gene Ontology (GO)
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