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Inflammatory myofibroblastic tumor
6 associated genes
No signs/symptoms info
PROTEIN INTERACTIONS: 1
Terminal osseous dysplasia - pigmentary defects
1 OMIM reference -
1 associated gene
No signs/symptoms info
Inflammatory myofibroblastic tumor
Terminal osseous dysplasia - pigmentary defects

ALK
(UniProt - OMIM)
 FLNA
(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)
RANBP2
(0.49)
FLNA


Citations in the biomedical literature:


Inflammatory myofibroblastic tumor
ALK CARS CLTC RANBP2 TPM3 TPM4

Terminal osseous dysplasia - pigmentary defects
FLNA



Inflammatory myofibroblastic tumor
Terminal osseous dysplasia - pigmentary defects

Classification (Orphanet):
- Rare oncologic disease
Classification (Orphanet):
- Rare bone disease
- Rare developmental defect during embryogenesis
- Rare genetic disease
- Rare skin disease
Classification (ICD10):
(no data available)
Classification (ICD10):
- Congenital malformations, deformations and chromosomal abnormalities -
Epidemiological data:
(no data available)
Epidemiological data:
Class of prevalence: <1 / 1 000 000
Average age onset: neonatal/infancy
Average age of death: normal
Type of inheritance: x-linked dominant
External references:
No OMIM references
No MeSH references
External references:
1 OMIM reference -
No MeSH references
No signs/symptoms info available.