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Autosomal dominant limb-girdle muscular dystrophy type 1B
1 OMIM reference -
1 associated gene
No signs/symptoms info
PROTEIN INTERACTIONS: 1
Familial primary hypomagnesemia with normocalcuria and normocalcemia
2 OMIM references -
2 associated genes
No signs/symptoms info
Autosomal dominant limb-girdle muscular dystrophy type 1B
Familial primary hypomagnesemia with normocalcuria and normocalcemia

LMNA
(UniProt - OMIM)
 CNNM2
(UniProt - OMIM)
EGF
(UniProt - OMIM)

INTERACTOME
ASSOCIATIONS
(click on a score value to see the evidence)
LMNA
(0.67)
EGF


Citations in the biomedical literature:


Autosomal dominant limb-girdle muscular dystrophy type 1B
LMNA
Familial primary hypomagnesemia with normocalcuria and normocalcemia
CNNM2 EGF



Autosomal dominant limb-girdle muscular dystrophy type 1B
Familial primary hypomagnesemia with normocalcuria and normocalcemia

Synonym(s):
- LGMD1B
- Limb-girdle muscular dystrophy due to lamin A/C deficiency
Synonym(s):
(no synonyms)
Classification (Orphanet):
- Rare cardiac disease
- Rare genetic disease
- Rare neurologic disease
Classification (Orphanet):
- Inborn errors of metabolism
- Rare genetic disease
- Rare renal disease
Classification (ICD10):
- Diseases of the nervous system -
Classification (ICD10):
- Endocrine, nutritional and metabolic diseases -
Epidemiological data:
Class of prevalence: 1-9 / 1 000 000
Average age onset: childhood
Average age of death: -
Type of inheritance: autosomal dominant
Epidemiological data:
Class of prevalence: <1 / 1 000 000
Average age onset: neonatal/infancy
Average age of death: any age
Type of inheritance: autosomal dominant
External references:
1 OMIM reference -
No MeSH references
External references:
2 OMIM references -
No MeSH references
No signs/symptoms info available.