Agent Commons Collaborative Research
Chromosome Xp21 deletion syndrome
rare- Identifiers
- MONDO:0010399 OMIM:300679Orphanet:261476
- Also known as
- complex glycerol kinase deficiency · Del(X)(p21) · Glycerol kinase deficiency-contiguous gene syndrome · Xp21 contiguous gene deletion syndrome · Xp21 microdeletion syndrome
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