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Disease Ontology Browser
chromosome Xp21 deletion syndrome (DOID:0060427)
Synonyms: complex glycerol kinase deficiency; monosomy Xp21; Xp21 microdeletion syndrome
Alt IDs: OMIM:300679, ICD10CM:Q99.8, ORDO:261476


Contributing Projects:
Mouse Genome Database (MGD), Gene Expression Database (GXD), Mouse Tumor Biology (MTB), Gene Ontology (GO), MouseCyc
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last database update
05/16/2017
MGI 6.09
The Jackson Laboratory