Cytoscape Web
Click node...

Hereditary sensorimotor neuropathy with hyperelastic skin
1 associated gene
No signs/symptoms info
PROTEIN INTERACTIONS: 1
Neonatal Marfan syndrome
1 associated gene
No signs/symptoms info
Hereditary sensorimotor neuropathy with hyperelastic skin
Neonatal Marfan syndrome

FBLN5
(UniProt - OMIM)
 FBN1
(UniProt - OMIM)

INTERACTOME
ASSOCIATIONS
(click on a score value to see the evidence)
FBLN5
(0.63)
FBN1


Citations in the biomedical literature:


Hereditary sensorimotor neuropathy with hyperelastic skin
FBLN5
Neonatal Marfan syndrome
FBN1



Hereditary sensorimotor neuropathy with hyperelastic skin
Neonatal Marfan syndrome

Synonym(s):
(no synonyms)

Synonym(s):
- Neonatal MFS
Classification (Orphanet):
- Rare genetic disease
- Rare neurologic disease
Classification (Orphanet):
- Rare circulatory system disease
- Rare genetic disease
- Rare surgical thoracic disease
- Rare systemic or rheumatologic disease
Classification (ICD10):
- Diseases of the nervous system -
Classification (ICD10):
- Congenital malformations, deformations and chromosomal abnormalities -
Epidemiological data:
Class of prevalence: <1 / 1 000 000
Average age onset: variable
Average age of death: -
Type of inheritance: autosomal dominant
Epidemiological data:
Class of prevalence: unknown
Average age onset: neonatal/infancy
Average age of death: -
Type of inheritance: autosomal dominant
External references:
No OMIM references
No MeSH references
External references:
No OMIM references
No MeSH references
No signs/symptoms info available.