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Congenital myopathy, Paradas type
1 associated gene
No signs/symptoms info
PROTEIN INTERACTIONS: 1
Chilblain lupus
2 OMIM references -
2 associated genes
No signs/symptoms info
Congenital myopathy, Paradas type
Chilblain lupus

DYSF
(UniProt - OMIM)
 SAMHD1
(UniProt - OMIM)
TREX1
(UniProt - OMIM)

INTERACTOME
ASSOCIATIONS
(click on a score value to see the evidence)
DYSF
(0.63)
SAMHD1


Citations in the biomedical literature:


Congenital myopathy, Paradas type
DYSF
Chilblain lupus
SAMHD1 TREX1



Congenital myopathy, Paradas type
Chilblain lupus

Classification (Orphanet):
- Rare genetic disease
- Rare neurologic disease
Classification (Orphanet):
- Rare genetic disease
- Rare skin disease
Classification (ICD10):
- Diseases of the nervous system -
Classification (ICD10):
- Diseases of the skin and subcutaneous tissue -
Epidemiological data:
(no data available)
Epidemiological data:
(no data available)
External references:
No OMIM references
No MeSH references
External references:
2 OMIM references -
1 MeSH reference: C535924
No signs/symptoms info available.