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Autosomal dominant spastic paraplegia type 3
1 OMIM reference -
1 associated gene
No signs/symptoms info
COMMON GENES: 1
Hereditary sensory and autonomic neuropathy type 1
4 OMIM references -
4 associated genes
No signs/symptoms info
Autosomal dominant spastic paraplegia type 3
Hereditary sensory and autonomic neuropathy type 1

ATL1
(UniProt - OMIM)
 ATL1
(UniProt - OMIM)
ATL3
(UniProt - OMIM)
SPTLC1
(UniProt - OMIM)
SPTLC2
(UniProt - OMIM)

COMMON
GENES 		ATL1


Citations in the biomedical literature:


Autosomal dominant spastic paraplegia type 3
ATL1
Hereditary sensory and autonomic neuropathy type 1
ATL3 SPTLC1 SPTLC2



Autosomal dominant spastic paraplegia type 3
Hereditary sensory and autonomic neuropathy type 1

Synonym(s):
- Strümpell disease
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):
- Diseases of the nervous system -
Epidemiological data:
(no data available)
Epidemiological data:
Class of prevalence: unknown
Average age onset: variable
Average age of death: -
Type of inheritance: autosomal dominant
External references:
1 OMIM reference -
1 MeSH reference: C536864
External references:
4 OMIM references -
No MeSH references
No signs/symptoms info available.