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Autosomal recessive spastic paraplegia type 20
1 OMIM reference -
1 associated gene
No signs/symptoms info
PROTEIN INTERACTIONS: 1
Autosomal dominant childhood-onset proximal spinal muscular atrophy without contractures
1 OMIM reference -
1 associated gene
No signs/symptoms info
Autosomal recessive spastic paraplegia type 20
Autosomal dominant childhood-onset proximal spinal muscular atrophy without contractures

SPG20
(UniProt - OMIM)
 DYNC1H1
(UniProt - OMIM)

INTERACTOME
ASSOCIATIONS
(click on a score value to see the evidence)
SPG20
(0.72)
DYNC1H1


Citations in the biomedical literature:


Autosomal recessive spastic paraplegia type 20
SPG20
Autosomal dominant childhood-onset proximal spinal muscular atrophy without contractures
DYNC1H1



Autosomal recessive spastic paraplegia type 20
Autosomal dominant childhood-onset proximal spinal muscular atrophy without contractures

Synonym(s):
- Childhood-onset spastic paraparesis - distal muscle wasting
- SPG20
- Troyer syndrome
Synonym(s):
- Lower extremity-predominant autosomal dominant proximal spinal muscular atrophy without contractures
- SMALED1
Classification (Orphanet):
- Rare genetic disease
- Rare neurologic disease
Classification (Orphanet):
- Rare genetic disease
- Rare neurologic disease
Classification (ICD10):
- Diseases of the nervous system -
Classification (ICD10):
- Diseases of the nervous system -
Epidemiological data:
Class of prevalence: -
Average age onset: -
Average age of death: -
Type of inheritance: autosomal recessive
Epidemiological data:
Class of prevalence: unknown
Average age onset: childhood
Average age of death: adult
Type of inheritance: autosomal dominant
External references:
1 OMIM reference -
No MeSH references
External references:
1 OMIM reference -
No MeSH references
No signs/symptoms info available.