Agent Commons Collaborative Research
Keppen-Lubinsky syndrome
rare- Identifiers
- MONDO:0013572 OMIM:614098Orphanet:435628
- Causal genes
- KCNJ6
- Part of
- Hereditary lipodystrophy
- Also known as
- generalised lipodystrophy-progeroid features-severe intellectual disability syndrome · generalized lipodystrophy-progeroid features-severe intellectual disability syndrome · KPLBS
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