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Inflammatory myofibroblastic tumor
6 associated genes
No signs/symptoms info
PROTEIN INTERACTIONS: 1
Lethal encephalopathy due to mitochondrial and peroxisomal fission defect
1 OMIM reference -
1 associated gene
No signs/symptoms info
Inflammatory myofibroblastic tumor
Lethal encephalopathy due to mitochondrial and peroxisomal fission defect

ALK
(UniProt - OMIM)
 DNM1L
(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)
CARS
(0.63)
DNM1L


Citations in the biomedical literature:


Inflammatory myofibroblastic tumor
ALK CARS CLTC RANBP2 TPM3 TPM4

Lethal encephalopathy due to mitochondrial and peroxisomal fission defect
DNM1L



Inflammatory myofibroblastic tumor
Lethal encephalopathy due to mitochondrial and peroxisomal fission defect

Classification (Orphanet):
- Rare oncologic disease
Classification (Orphanet):
- Inborn errors of metabolism
- Rare genetic disease
- Rare neurologic disease
Classification (ICD10):
(no data available)
Classification (ICD10):
(no data available)
Epidemiological data:
(no data available)
Epidemiological data:
Class of prevalence: <1 / 1 000 000
Average age onset: neonatal/infancy
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.