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1 associated gene
No signs/symptoms info
COMMON GENES: 1
1 OMIM reference -
1 associated gene
No signs/symptoms info
Progeroid and marfanoid aspect-lipodystrophy syndrome
Marfan syndrome type 1

FBN1 FBN1


COMMON
GENES
FBN1



Citations in the biomedical literature:


Progeroid and marfanoid aspect-lipodystrophy syndrome
FBN1
Marfan syndrome type 1



Progeroid and marfanoid aspect-lipodystrophy syndrome
Marfan syndrome type 1

Synonym(s):
(no synonyms)

Synonym(s):
- MFS1

Classification (Orphanet):
- Rare genetic disease
- Rare systemic or rheumatologic disease
Classification (Orphanet):
- Rare circulatory system disease
- Rare genetic disease
- Rare surgical thoracic disease
- Rare systemic or rheumatologic disease

Classification (ICD10):
- Endocrine, nutritional and metabolic diseases -
Classification (ICD10):
- Congenital malformations, deformations and chromosomal abnormalities -

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

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

No signs/symptoms info available.