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Autosomal dominant Emery-Dreifuss muscular dystrophy
4 OMIM references -
4 associated genes
No signs/symptoms info
PROTEIN INTERACTIONS: 1
Autosomal dominant optic atrophy, classic type
3 OMIM references -
1 associated gene
No signs/symptoms info
Autosomal dominant Emery-Dreifuss muscular dystrophy
Autosomal dominant optic atrophy, classic type

LMNA
(UniProt - OMIM)
 OPA1
(UniProt - OMIM)
SYNE1
(UniProt - OMIM)
SYNE2
(UniProt - OMIM)
TMEM43
(UniProt - OMIM)

INTERACTOME
ASSOCIATIONS
(click on a score value to see the evidence)
LMNA
(0.63)
OPA1


Citations in the biomedical literature:


Autosomal dominant Emery-Dreifuss muscular dystrophy
LMNA SYNE1 SYNE2 TMEM43
Autosomal dominant optic atrophy, classic type
OPA1



Autosomal dominant Emery-Dreifuss muscular dystrophy
Autosomal dominant optic atrophy, classic type

Synonym(s):
(no synonyms)

Synonym(s):
- Autosomal dominant optic atrophy, Kjer type
- Kjer disease
Classification (Orphanet):
- Rare cardiac disease
- Rare genetic disease
- Rare neurologic disease
Classification (Orphanet):
- Inborn errors of metabolism
- Rare eye disease
- Rare genetic disease
Classification (ICD10):
- Diseases of the nervous system -
Classification (ICD10):
- Diseases of the eye and adnexa -
Epidemiological data:
(no data available)
Epidemiological data:
Class of prevalence: -
Average age onset: childhood
Average age of death: -
Type of inheritance: autosomal dominant
External references:
4 OMIM references -
No MeSH references
External references:
3 OMIM references -
No MeSH references
No signs/symptoms info available.