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Keppen-Lubinsky syndrome

Disease Summary
Associated Targets (1)
Tchem

1


Uniprot Description A rare disease characterized by severe developmental delay, intellectual disability, severe generalized lipodystrophy, dysmorphic features including microcephaly, large prominent eyes, narrow nasal bridge, tented upper lip, high palate, open mouth, tightly adherent skin, and aged appearance.
Mondo Term and Equivalent IDs
MONDO:0013572:  Keppen-Lubinsky syndrome
Orphanet:435628: 
UMLS:C3279800: