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Cardiomyopathy - hypotonia - lactic acidosis
1 OMIM reference -
1 associated gene
No signs/symptoms info
PROTEIN INTERACTIONS: 1
Autosomal recessive spastic paraplegia type 7
2 OMIM references -
1 associated gene
No signs/symptoms info
Cardiomyopathy - hypotonia - lactic acidosis
Autosomal recessive spastic paraplegia type 7

SLC25A3
(UniProt - OMIM)
 SPG7
(UniProt - OMIM)

INTERACTOME
ASSOCIATIONS
(click on a score value to see the evidence)
SLC25A3
(0.49)
SPG7


Citations in the biomedical literature:


Cardiomyopathy - hypotonia - lactic acidosis
SLC25A3
Autosomal recessive spastic paraplegia type 7
SPG7



Cardiomyopathy - hypotonia - lactic acidosis
Autosomal recessive spastic paraplegia type 7

Synonym(s):
(no synonyms)

Synonym(s):
- SPG7
Classification (Orphanet):
- Inborn errors of metabolism
- Rare cardiac disease
- Rare genetic disease
Classification (Orphanet):
- Inborn errors of metabolism
- Rare eye disease
- Rare genetic disease
- Rare neurologic disease
Classification (ICD10):
- Diseases of the nervous system -
Classification (ICD10):
- Diseases of the nervous system -
Epidemiological data:
(no data available)
Epidemiological data:
Class of prevalence: 1-9 / 100 000
Average age onset: variable
Average age of death: -
Type of inheritance: autosomal recessive
External references:
1 OMIM reference -
No MeSH references
External references:
2 OMIM references -
No MeSH references
No signs/symptoms info available.