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Autosomal dominant limb-girdle muscular dystrophy type 1A
1 OMIM reference -
1 associated gene
No signs/symptoms info
PROTEIN INTERACTIONS: 1
Early-onset autosomal dominant Alzheimer disease
16 OMIM references -
4 associated genes
No signs/symptoms info
Autosomal dominant limb-girdle muscular dystrophy type 1A
Early-onset autosomal dominant Alzheimer disease

MYOT
(UniProt - OMIM)
 APP
(UniProt - OMIM)
PSEN1
(UniProt - OMIM)
PSEN2
(UniProt - OMIM)
SORL1
(UniProt - OMIM)

INTERACTOME
ASSOCIATIONS
(click on a score value to see the evidence)
MYOT
(0.56)
APP


Citations in the biomedical literature:


Autosomal dominant limb-girdle muscular dystrophy type 1A
MYOT
Early-onset autosomal dominant Alzheimer disease
APP PSEN1 PSEN2 SORL1



Autosomal dominant limb-girdle muscular dystrophy type 1A
Early-onset autosomal dominant Alzheimer disease

Synonym(s):
- LGMD1A
- Limb-girdle muscular dystrophy due to myotilin deficiency
Synonym(s):
- EOFAD
- Early-onset familial autosomal dominant Alzheimer disease
- Familial Alzheimer disease
Classification (Orphanet):
- Rare genetic disease
- Rare neurologic disease
Classification (Orphanet):
- Rare genetic disease
- Rare neurologic disease
Classification (ICD10):
- Diseases of the nervous system -
Classification (ICD10):
- Diseases of the nervous system -
Epidemiological data:
Class of prevalence: <1 / 1 000 000
Average age onset: adulthood
Average age of death: normal
Type of inheritance: autosomal dominant
Epidemiological data:
Class of prevalence: 1-9 / 100 000
Average age onset: adulthood
Average age of death: adult
Type of inheritance: autosomal dominant
External references:
1 OMIM reference -
No MeSH references
External references:
16 OMIM references -
No MeSH references
No signs/symptoms info available.