ODCs

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1 OMIM reference -
1 associated gene
No signs/symptoms info

COMMON GENES: 1

CANDLE syndrome

1 OMIM reference -
1 associated gene
No signs/symptoms info

JMP syndrome

CANDLE syndrome

PSMB8

(UniProt - OMIM)

(UniProt - OMIM)


COMMON GENES	PSMB8

Citations in the biomedical literature:

JMP syndrome		CANDLE syndrome
	Synonym(s): - Joint contractures-muscular atrophy-microcytic anemia-panniculitis-associated lipodystrophy syndrome		Synonym(s): - Chromic atypical neutrophilic dermatosis-lipodystrophy-elevated temperature 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: childhood Average age of death: no data available Type of inheritance: autosomal recessive		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

	External references: 1 OMIM reference - No MeSH references		External references: 1 OMIM reference - No MeSH references

No signs/symptoms info available.