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Progeroid and marfanoid aspect-lipodystrophy syndrome
1 associated gene
No signs/symptoms info
PROTEIN INTERACTIONS: 1
Hereditary sensorimotor neuropathy with hyperelastic skin
1 associated gene
No signs/symptoms info
Progeroid and marfanoid aspect-lipodystrophy syndrome
Hereditary sensorimotor neuropathy with hyperelastic skin

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

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


Citations in the biomedical literature:


Progeroid and marfanoid aspect-lipodystrophy syndrome
FBN1
Hereditary sensorimotor neuropathy with hyperelastic skin
FBLN5



Progeroid and marfanoid aspect-lipodystrophy syndrome
Hereditary sensorimotor neuropathy with hyperelastic skin

Classification (Orphanet):
- Rare genetic disease
- Rare systemic or rheumatologic disease
Classification (Orphanet):
- Rare genetic disease
- Rare neurologic disease
Classification (ICD10):
- Endocrine, nutritional and metabolic diseases -
Classification (ICD10):
- Diseases of the nervous system -
Epidemiological data:
Class of prevalence: <1 / 1 000 000
Average age onset: neonatal/infancy
Average age of death: no data available
Type of inheritance: autosomal dominant
Epidemiological data:
Class of prevalence: <1 / 1 000 000
Average age onset: variable
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.