disease has feature Joint stiffness Lipodystrophy Joint contracture of the hand immune system disorder autosomal recessive disease proteosome-associated autoinflammatory syndrome https://github.com/monarch-initiative/mondo/issues/6747 https://github.com/monarch-initiative/mondo/issues/7365 https://rarediseases.info.nih.gov/diseases/10811/chronic-atypical-neutrophilic-dermatosis-with-lipodystrophy-and-elevated-temperature https://rarediseases.info.nih.gov/diseases/10988/jmp-syndrome https://www.malacards.org/card/proteasome_associated_autoinflammatory_syndrome_1 https://www.malacards.org/card/proteosome_associated_autoinflammatory_syndrome DOID:0050553 JMP syndrome Joint contractures - muscle atrophy - microcytic anaemia - panniculitis-induced lipodystrophy ALDD NANDO:2200435 NNS Orphanet:325004 Nakajo syndrome MEDGEN:376827 Orphanet:324999 UMLS:C1850568 secondary hypertrophic osteoperiostosis with pernio PRAAS proteasome disability syndrome Orphanet:2615 DOID:0060913 OMIMPS:256040 ALDD syndrome autoinflammation, lipodystrophy, and dermatosis syndrome Joint contractures, muscular atrophy, microcytic Anemia, and panniculitis-induced lipodystrophy MESH:C538334 NANDO:1200867 Nakajo-Nishimura syndrome chronic atypical neutrophilic dermatosis with lipodystrophy and elevated temperature Nakajo Nishimura syndrome chronic atypical neutrophilic dermatosis with lipodystrophy and elevated temperature syndrome Orphanet:324977 chronic atypical neutrophilic dermatosis-lipodystrophy-elevated temperature syndrome CANDLE syndrome amyotrophy fat tissue anomaly Joint contractures-muscular atrophy-microcytic anemia-panniculitis-associated lipodystrophy syndrome proteasome-associated autoinflammatory syndrome amyotrophy-fat tissue anomaly syndrome ICD9:709.8 GARD:0013824 autoinflammation-lipodystrophy-dermatosis syndrome nodular erythema digital changes joint contractures, muscular atrophy, microcytic anemia, and panniculitis-induced lipodystrophy SCTID:702449004 Joint contractures - muscle atrophy - microcytic anemia - panniculitis-induced lipodystrophy MONDO:0009726 hereditary disorder of connective tissue type 1 interferonopathy of childhood