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1 OMIM reference -
1 associated gene
No signs/symptoms info
PROTEIN INTERACTIONS: 1
4 associated genes
No signs/symptoms info
Recessive hereditary methemoglobinemia type 2
Pediatric systemic lupus erythematosus

CYB5R3 IRAK1
PTPN22
SPP1
STAT4


INTERACTOME
ASSOCIATIONS

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



Citations in the biomedical literature:


Recessive hereditary methemoglobinemia type 2
CYB5R3
Pediatric systemic lupus erythematosus
IRAK1 PTPN22 SPP1 STAT4



Recessive hereditary methemoglobinemia type 2
Pediatric systemic lupus erythematosus

Synonym(s):
- NADH-cytochrome b5reductase deficiency type 2
- NADH-diaphorase deficiency type 2
- Recessive congenital methemoglobinemia type 2

Synonym(s):
- SLE, pediatric onset

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

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

Epidemiological data:
Class of prevalence: <1 / 1 000 000
Average age onset: neonatal/infancy
Average age of death: young adult
Type of inheritance: autosomal recessive
Epidemiological data:
(no data available)

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

No signs/symptoms info available.