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1 OMIM reference -
1 associated gene
No signs/symptoms info
PROTEIN INTERACTIONS: 1
1 OMIM reference -
7 associated genes
No signs/symptoms info
Autosomal dominant limb-girdle muscular dystrophy type 1B
Translocation renal cell carcinoma

LMNA ASPSCR1
CLTC
NONO
PRCC
SFPQ
TFE3
TFEB


INTERACTOME
ASSOCIATIONS

(click on a score value to see the evidence)
LMNA
(0.59)
NONO



Citations in the biomedical literature:


Autosomal dominant limb-girdle muscular dystrophy type 1B
LMNA
Translocation renal cell carcinoma
ASPSCR1 CLTC NONO PRCC SFPQ TFE3
TFEB



Autosomal dominant limb-girdle muscular dystrophy type 1B
Translocation renal cell carcinoma

Synonym(s):
- LGMD1B
- Limb-girdle muscular dystrophy due to lamin A/C deficiency

Synonym(s):
- Carcinoma associated with MITF/TFE translocation
- Translocation carcinoma

Classification (Orphanet):
- Rare cardiac disease
- Rare genetic disease
- Rare neurologic disease
Classification (Orphanet):
- Rare oncologic disease
- Rare renal disease

Classification (ICD10):
- Diseases of the nervous system -
Classification (ICD10):
- Neoplasms -

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:
(no data available)

External references:
1 OMIM reference -
No MeSH references
External references:
1 OMIM reference -
No MeSH references

No signs/symptoms info available.