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Autosomal dominant limb-girdle muscular dystrophy type 1C
1 OMIM reference -
1 associated gene
No signs/symptoms info
PROTEIN INTERACTIONS: 1
Myeloid neoplasm associated with PDGFRB rearrangement
1 associated gene
No signs/symptoms info
Autosomal dominant limb-girdle muscular dystrophy type 1C
Myeloid neoplasm associated with PDGFRB rearrangement

CAV3
(UniProt - OMIM)
 PDGFRB
(UniProt - OMIM)

INTERACTOME
ASSOCIATIONS
(click on a score value to see the evidence)
CAV3
(0.75)
PDGFRB


Citations in the biomedical literature:


Autosomal dominant limb-girdle muscular dystrophy type 1C
CAV3
Myeloid neoplasm associated with PDGFRB rearrangement
PDGFRB



Autosomal dominant limb-girdle muscular dystrophy type 1C
Myeloid neoplasm associated with PDGFRB rearrangement

Synonym(s):
- LGMD1C
- Limb-girdle muscular dystrophy due to caveolin-3 deficiency
Synonym(s):
(no synonyms)
Classification (Orphanet):
- Rare genetic disease
- Rare neurologic disease
Classification (Orphanet):
- Rare hematologic disease
- Rare oncologic disease
Classification (ICD10):
- Diseases of the nervous system -
Classification (ICD10):
(no data available)
Epidemiological data:
Class of prevalence: <1 / 1 000 000
Average age onset: childhood
Average age of death: normal
Type of inheritance: autosomal dominant
Epidemiological data:
(no data available)
External references:
1 OMIM reference -
No MeSH references
External references:
No OMIM references
No MeSH references
No signs/symptoms info available.