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Charcot-Marie-Tooth disease type 4D
1 OMIM reference -
1 associated gene
No signs/symptoms info
PROTEIN INTERACTIONS: 1
Melanoma of soft part
3 associated genes
No signs/symptoms info
Charcot-Marie-Tooth disease type 4D
Melanoma of soft part

NDRG1
(UniProt - OMIM)
 ATF1
(UniProt - OMIM)
CREB1
(UniProt - OMIM)
EWSR1
(UniProt - OMIM)

INTERACTOME
ASSOCIATIONS
(click on a score value to see the evidence)
NDRG1
(0.73)
EWSR1


Citations in the biomedical literature:


Charcot-Marie-Tooth disease type 4D
NDRG1
Melanoma of soft part
ATF1 CREB1 EWSR1



Charcot-Marie-Tooth disease type 4D
Melanoma of soft part

Synonym(s):
- CMT4D
- HMSN, Lom type
- Hereditary motor and sensory neuropathy, Lom type
Synonym(s):
- Clear cell sarcoma of soft tissue
- Clear cell sarcoma of the tendons and aponeuroses
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: unknown
Average age onset: childhood
Average age of death: -
Type of inheritance: autosomal recessive
Epidemiological data:
(no data available)
External references:
1 OMIM reference -
1 MeSH reference: C535716
External references:
No OMIM references
No MeSH references
No signs/symptoms info available.