ODCs

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4 associated genes
No signs/symptoms info

PROTEIN INTERACTIONS: 1

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

Pediatric systemic lupus erythematosus

Recessive hereditary methemoglobinemia type 1


INTERACTOME ASSOCIATIONS (click on a score value to see the evidence)	SPP1	(0.63)	CYB5R3

Citations in the biomedical literature:

Pediatric systemic lupus erythematosus		Recessive hereditary methemoglobinemia type 1
	Synonym(s): - SLE, pediatric onset		Synonym(s): - NADH-cytochrome b5reductase deficiency type 1 - NADH-diaphorase deficiency type 1 - Recessive congenital methemoglobinemia type 1

	Classification (Orphanet): - Rare neurologic disease - Rare renal disease - Rare respiratory disease - Rare systemic or rheumatologic disease		Classification (Orphanet): - Rare genetic disease - Rare hematologic disease

	Classification (ICD10): - Diseases of the musculoskeletal system and connective tissue -		Classification (ICD10): - Diseases of the blood and blood-forming organs and certain disorders involving the immune mechanism -

	Epidemiological data: (no data available)		Epidemiological data: Class of prevalence: unknown Average age onset: neonatal/infancy Average age of death: normal Type of inheritance: autosomal recessive

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

No signs/symptoms info available.