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1 associated gene
No signs/symptoms info
PROTEIN INTERACTIONS: 1
1 associated gene
No signs/symptoms info
Laminopathy type Decaudain-Vigouroux
Unilateral retinoblastoma

LMNA RB1


INTERACTOME
ASSOCIATIONS

(click on a score value to see the evidence)
LMNA
(0.86)
RB1



Citations in the biomedical literature:


Laminopathy type Decaudain-Vigouroux
LMNA
Unilateral retinoblastoma
RB1



Laminopathy type Decaudain-Vigouroux
Unilateral retinoblastoma

Synonym(s):
- Laminopathy with severe metabolic syndrome and myopathy

Synonym(s):
- Non-familial retinoblastoma
- Non-hereditary retinoblastoma

Classification (Orphanet):
- Rare endocrine disease
- Rare genetic disease
Classification (Orphanet):
- Rare eye disease
- Rare genetic disease
- Rare oncologic disease

Classification (ICD10):
- Endocrine, nutritional and metabolic diseases -
Classification (ICD10):
- Neoplasms -

Epidemiological data:
(no data available)
Epidemiological data:
Class of prevalence: unknown
Average age onset: neonatal/infancy
Average age of death: any age
Type of inheritance: sporadic

External references:
No OMIM references
No MeSH references
External references:
No OMIM references
No MeSH references

No signs/symptoms info available.