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CANDLE syndrome
1 OMIM reference -
1 associated gene
No signs/symptoms info
COMMON GENES: 1
JMP syndrome
1 OMIM reference -
1 associated gene
No signs/symptoms info
CANDLE syndrome
JMP syndrome

PSMB8
(UniProt - OMIM)
 PSMB8
(UniProt - OMIM)

COMMON
GENES 		PSMB8


Citations in the biomedical literature:


CANDLE syndrome
PSMB8
JMP syndrome



CANDLE syndrome
JMP syndrome

Synonym(s):
- Chromic atypical neutrophilic dermatosis-lipodystrophy-elevated temperature syndrome
Synonym(s):
- Joint contractures-muscular atrophy-microcytic anemia-panniculitis-associated lipodystrophy syndrome
Classification (Orphanet):
- Rare genetic disease
- Rare skin disease
- Rare systemic or rheumatologic disease
Classification (Orphanet):
- Rare genetic disease
- Rare skin disease
- Rare systemic or rheumatologic disease
Classification (ICD10):
(no data available)
Classification (ICD10):
(no data available)
Epidemiological data:
Class of prevalence: <1 / 1 000 000
Average age onset: neonatal/infancy
Average age of death: any age
Type of inheritance: autosomal recessive
Epidemiological data:
Class of prevalence: <1 / 1 000 000
Average age onset: childhood
Average age of death: no data available
Type of inheritance: autosomal recessive
External references:
1 OMIM reference -
No MeSH references
External references:
1 OMIM reference -
No MeSH references
No signs/symptoms info available.