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1 OMIM reference -
1 associated gene
No signs/symptoms info
PROTEIN INTERACTIONS: 1
Autosomal dominant spastic paraplegia type 13
Mendelian susceptibility to mycobacterial diseases due to complete ISG15 deficiency

HSPD1 ISG15


INTERACTOME
ASSOCIATIONS

(click on a score value to see the evidence)
HSPD1
(0.63)
ISG15



Citations in the biomedical literature:


Autosomal dominant spastic paraplegia type 13
HSPD1
Mendelian susceptibility to mycobacterial diseases due to complete ISG15 deficiency
ISG15



Autosomal dominant spastic paraplegia type 13
Mendelian susceptibility to mycobacterial diseases due to complete ISG15 deficiency

Synonym(s):
- SPG13

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

Classification (Orphanet):
- Rare genetic disease
- Rare neurologic disease
Classification (Orphanet):
- Rare genetic disease
- Rare immune disease

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

Epidemiological data:
Class of prevalence: <1 / 1 000 000
Average age onset: -
Average age of death: -
Type of inheritance: autosomal dominant
Epidemiological data:
Class of prevalence: <1 / 1 000 000
Average age onset: childhood
Average age of death: normal
Type of inheritance: autosomal recessive

External references:
1 OMIM reference -
1 MeSH reference: C537485
External references:
No OMIM references
No MeSH references

No signs/symptoms info available.