Search Ontology:
Human Disease

proteasome-associated autoinflammatory syndrome 1

Term ID
DOID:0050553
Synonyms
  • CANDLE
  • chronic atypical neutrophilic dermatosis with lipodystrophy and elevated temperature syndrome
  • JMP syndrome
  • JOINT CONTRACTURES, MUSCULAR ATROPHY, MICROCYTIC ANEMIA, AND PANNICULITIS-INDUCED LIPODYSTROPHY
  • Nakajo-Nishimura syndrome
  • NKJO
  • PRAAS1
Definition
A proteasome-associated autoinflammatory syndrome that is characterized by early childhood onset of annular erythematous plaques on the face and extremities with subsequent development of partial lipodystrophy and laboratory evidence of immune dysregulation and that has_material_basis_in homozygous mutation in the PSMB8 gene on chromosome 6p21 or a heterozygous mutation in the PSMB8 gene and a heterozygous mutation in either the PSMA3 gene on chromosome 14q23 or in the PSMB4 gene on chromosome 1q21. (4)
References
  • GARD:10988
  • GARD:3916
  • GARD:3917
  • MIM:256040
  • ORDO:324999
Ontology
Human Disease   ( DOID:0050553 )
Relationships
is a type of
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Genes Involved
Zebrafish Models