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Autosomal dominant Emery-Dreifuss muscular dystrophy
4 OMIM references -
4 associated genes
No signs/symptoms info
COMMON GENES: 1
PROTEIN INTERACTIONS: 1
Atypical Werner syndrome
1 associated gene
No signs/symptoms info
Autosomal dominant Emery-Dreifuss muscular dystrophy
Atypical Werner syndrome

LMNA
(UniProt - OMIM)
 LMNA
(UniProt - OMIM)
SYNE1
(UniProt - OMIM)
SYNE2
(UniProt - OMIM)
TMEM43
(UniProt - OMIM)

COMMON
GENES 		LMNA
INTERACTOME
ASSOCIATIONS
(click on a score value to see the evidence)
SYNE1
(0.88)
LMNA


Citations in the biomedical literature:


Autosomal dominant Emery-Dreifuss muscular dystrophy
LMNA SYNE1 SYNE2 TMEM43
Atypical Werner syndrome



Autosomal dominant Emery-Dreifuss muscular dystrophy
Atypical Werner syndrome

Synonym(s):
(no synonyms)

Synonym(s):
- Atypical progeroid syndrome
Classification (Orphanet):
- Rare cardiac disease
- Rare genetic disease
- Rare neurologic disease
Classification (Orphanet):
- Rare developmental defect during embryogenesis
- Rare genetic disease
Classification (ICD10):
- Diseases of the nervous system -
Classification (ICD10):
- Endocrine, nutritional and metabolic diseases -
Epidemiological data:
(no data available)
Epidemiological data:
(no data available)
External references:
4 OMIM references -
No MeSH references
External references:
No OMIM references
No MeSH references
No signs/symptoms info available.