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

ALK
(UniProt - OMIM)
 SPG20
(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)
CLTC
(0.72)
SPG20


Citations in the biomedical literature:


Inflammatory myofibroblastic tumor
ALK CARS CLTC RANBP2 TPM3 TPM4

Autosomal recessive spastic paraplegia type 20
SPG20



Inflammatory myofibroblastic tumor
Autosomal recessive spastic paraplegia type 20

Synonym(s):
(no synonyms)

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