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1 OMIM reference -
1 associated gene
No signs/symptoms info
PROTEIN INTERACTIONS: 1
1 OMIM reference -
1 associated gene
No signs/symptoms info
Nestor-Guillermo progeria syndrome
Familial dilated cardiomyopathy with conduction defect due to LMNA mutation

BANF1 LMNA


INTERACTOME
ASSOCIATIONS

(click on a score value to see the evidence)
BANF1
(0.63)
LMNA



Citations in the biomedical literature:


Nestor-Guillermo progeria syndrome
BANF1
Familial dilated cardiomyopathy with conduction defect due to LMNA mutation
LMNA



Nestor-Guillermo progeria syndrome
Familial dilated cardiomyopathy with conduction defect due to LMNA mutation

Synonym(s):
- NGPS

Synonym(s):
(no synonyms)

Classification (Orphanet):
- Rare bone disease
- Rare developmental defect during embryogenesis
- Rare genetic disease
- Rare skin disease
Classification (Orphanet):
- Rare cardiac disease
- Rare genetic disease

Classification (ICD10):
- Endocrine, nutritional and metabolic diseases -
Classification (ICD10):
(no data available)

Epidemiological data:
Class of prevalence: <1 / 1 000 000
Average age onset: childhood
Average age of death: -
Type of inheritance: autosomal recessive
Epidemiological data:
Class of prevalence: unknown
Average age onset: -
Average age of death: -
Type of inheritance: autosomal dominant

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

No signs/symptoms info available.