Cytoscape Web
Click node...


1 OMIM reference -
1 associated gene
No signs/symptoms info
PROTEIN INTERACTIONS: 1
2 OMIM references -
3 associated genes
No signs/symptoms info
Autosomal dominant spastic paraplegia type 13
Genetic recurrent myoglobinuria

HSPD1 LPIN1
MT-CO1
MT-CO3


INTERACTOME
ASSOCIATIONS

(click on a score value to see the evidence)
HSPD1
(0.55)
MT-CO1



Citations in the biomedical literature:


Autosomal dominant spastic paraplegia type 13
HSPD1
Genetic recurrent myoglobinuria
LPIN1 MT-CO1 MT-CO3



Autosomal dominant spastic paraplegia type 13
Genetic recurrent myoglobinuria

Synonym(s):
- SPG13

Synonym(s):
(no synonyms)

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

Classification (ICD10):
- Diseases of the nervous system -
Classification (ICD10):
- Symptoms, signs and abnormal clinical and laboratory findings, not elsewhere classified -

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: unknown
Average age onset: childhood
Average age of death: -
Type of inheritance: autosomal dominant

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

No signs/symptoms info available.