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6 associated genes
No signs/symptoms info
PROTEIN INTERACTIONS: 1
1 OMIM reference -
1 associated gene
No signs/symptoms info
Inflammatory myofibroblastic tumor
Distal myopathy with vocal cord weakness

ALK MATR3
CARS
CLTC
RANBP2
TPM3
TPM4


INTERACTOME
ASSOCIATIONS

(click on a score value to see the evidence)
RANBP2
(0.49)
MATR3



Citations in the biomedical literature:


Inflammatory myofibroblastic tumor
ALK CARS CLTC RANBP2 TPM3 TPM4

Distal myopathy with vocal cord weakness
MATR3



Inflammatory myofibroblastic tumor
Distal myopathy with vocal cord weakness

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: <1 / 1 000 000
Average age onset: adulthood
Average age of death: -
Type of inheritance: autosomal dominant

External references:
No OMIM references
No MeSH references
External references:
1 OMIM reference -
No MeSH references

No signs/symptoms info available.