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proteosome-associated autoinflammatory syndrome

Disease Summary
Associated Targets (3)
Tclin

1

Tchem

1

Tbio

1


GARD Rare
Disease Ontology Description An autosomal recessive disease that is characterized by childhood onset of joint stiffness and severe contractures of the hands and feet, erythematous skin lesions with subsequent development of severe lipodystrophy.
Mondo Term and Equivalent IDs
MONDO:0009726:  proteosome-associated autoinflammatory syndrome
GARD:0003917: 
MESH:C538334: 
OMIMPS:256040: 
Orphanet:2615: 
Orphanet:324977: 
Orphanet:324999: 
SCTID:702449004: 
UMLS:CN202195: 
UMLS:CN204109: