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Lethal encephalopathy due to mitochondrial and peroxisomal fission defect
1 OMIM reference -
1 associated gene
No signs/symptoms info
PROTEIN INTERACTIONS: 1
Autosomal dominant spastic paraplegia type 13
1 OMIM reference -
1 associated gene
No signs/symptoms info
Lethal encephalopathy due to mitochondrial and peroxisomal fission defect
Autosomal dominant spastic paraplegia type 13

DNM1L
(UniProt - OMIM)
 HSPD1
(UniProt - OMIM)

INTERACTOME
ASSOCIATIONS
(click on a score value to see the evidence)
DNM1L
(0.55)
HSPD1


Citations in the biomedical literature:


Lethal encephalopathy due to mitochondrial and peroxisomal fission defect
DNM1L
Autosomal dominant spastic paraplegia type 13
HSPD1



Lethal encephalopathy due to mitochondrial and peroxisomal fission defect
Autosomal dominant spastic paraplegia type 13

Synonym(s):
(no synonyms)

Synonym(s):
- SPG13
Classification (Orphanet):
- Inborn errors of metabolism
- Rare genetic disease
- Rare neurologic disease
Classification (Orphanet):
- Rare genetic disease
- Rare neurologic disease
Classification (ICD10):
(no data available)
Classification (ICD10):
- Diseases of the nervous system -
Epidemiological data:
Class of prevalence: <1 / 1 000 000
Average age onset: neonatal/infancy
Average age of death: -
Type of inheritance: autosomal dominant
Epidemiological data:
Class of prevalence: <1 / 1 000 000
Average age onset: -
Average age of death: -
Type of inheritance: autosomal dominant
External references:
1 OMIM reference -
No MeSH references
External references:
1 OMIM reference -
1 MeSH reference: C537485
No signs/symptoms info available.