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Autosomal recessive spastic paraplegia type 20
1 OMIM reference -
1 associated gene
No signs/symptoms info
PROTEIN INTERACTIONS: 1
Inflammatory myofibroblastic tumor
6 associated genes
No signs/symptoms info
Autosomal recessive spastic paraplegia type 20
Inflammatory myofibroblastic tumor

SPG20
(UniProt - OMIM)
 ALK
(UniProt - OMIM)
CARS
(UniProt - OMIM)
CLTC
(UniProt - OMIM)
RANBP2
(UniProt - OMIM)
TPM3
(UniProt - OMIM)
TPM4
(UniProt - OMIM)

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


Citations in the biomedical literature:


Autosomal recessive spastic paraplegia type 20
SPG20
Inflammatory myofibroblastic tumor
ALK CARS CLTC RANBP2 TPM3 TPM4



Autosomal recessive spastic paraplegia type 20
Inflammatory myofibroblastic tumor

Synonym(s):
- Childhood-onset spastic paraparesis - distal muscle wasting
- SPG20
- Troyer syndrome
Synonym(s):
(no synonyms)
Classification (Orphanet):
- Rare genetic disease
- Rare neurologic disease
Classification (Orphanet):
- Rare oncologic disease
Classification (ICD10):
- Diseases of the nervous system -
Classification (ICD10):
(no data available)
Epidemiological data:
Class of prevalence: -
Average age onset: -
Average age of death: -
Type of inheritance: autosomal recessive
Epidemiological data:
(no data available)
External references:
1 OMIM reference -
No MeSH references
External references:
No OMIM references
No MeSH references
No signs/symptoms info available.