Search Ontology:
Human Disease

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
Ontology
Human Disease   ( DOID:0060427 )
Relationships
is a type of
Other Pages
Alliance (1)
Genes Involved
Zebrafish Models
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