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1 OMIM reference -
1 associated gene
No signs/symptoms info
PROTEIN INTERACTIONS: 1
14 OMIM references -
17 associated genes
No signs/symptoms info
Autosomal dominant limb-girdle muscular dystrophy type 1B
Familial atrial fibrillation

LMNA ABCC9
GATA4
GATA5
GATA6
GJA5
KCNA5
KCNE1
KCNE2
KCNJ2
KCNQ1
NKX2-5
NPPA
NUP155
PITX2
SCN1B
SCN2B
SCN5A


INTERACTOME
ASSOCIATIONS

(click on a score value to see the evidence)
LMNA
(0.49)
NUP155



Citations in the biomedical literature:


Autosomal dominant limb-girdle muscular dystrophy type 1B
LMNA
Familial atrial fibrillation
ABCC9 GATA4 GATA5 GATA6 GJA5 KCNA5
KCNE1 KCNE2 KCNJ2 KCNQ1 NKX2-5 NPPA
NUP155 PITX2 SCN1B SCN2B SCN5A



Autosomal dominant limb-girdle muscular dystrophy type 1B
Familial atrial fibrillation

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):
- Rare cardiac disease
- Rare genetic disease

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

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: -
Average age onset: -
Average age of death: -
Type of inheritance: autosomal dominant

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

No signs/symptoms info available.