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PROTEIN INTERACTIONS: 1
3 OMIM references -
4 associated genes
No signs/symptoms info
Mendelian susceptibility to mycobacterial diseases due to complete ISG15 deficiency
Isolated ATP synthase deficiency

ISG15 ATP5A1
ATP5E
ATPAF1
ATPAF2


INTERACTOME
ASSOCIATIONS

(click on a score value to see the evidence)
ISG15
(0.63)
ATP5A1



Citations in the biomedical literature:


Mendelian susceptibility to mycobacterial diseases due to complete ISG15 deficiency
ISG15
Isolated ATP synthase deficiency
ATP5A1 ATP5E ATPAF1 ATPAF2



Mendelian susceptibility to mycobacterial diseases due to complete ISG15 deficiency
Isolated ATP synthase deficiency

Synonym(s):
- MSMD due to complete ISG15 deficiency

Synonym(s):
- Isolated mitochondrial respiratory chain complex V deficiency

Classification (Orphanet):
- Rare genetic disease
- Rare immune disease
Classification (Orphanet):
- Inborn errors of metabolism
- Rare genetic disease

Classification (ICD10):
- Diseases of the blood and blood-forming organs and certain disorders involving the immune mechanism -
Classification (ICD10):
(no data available)

Epidemiological data:
Class of prevalence: <1 / 1 000 000
Average age onset: childhood
Average age of death: normal
Type of inheritance: autosomal recessive
Epidemiological data:
(no data available)

External references:
No OMIM references
No MeSH references
External references:
3 OMIM references -
No MeSH references

No signs/symptoms info available.