Cytoscape Web
Click node...

Synpolydactyly type 2
1 OMIM reference -
1 associated gene
No signs/symptoms info
PROTEIN INTERACTIONS: 1
Primary systemic amyloidosis
1 OMIM reference -
1 associated gene
No signs/symptoms info
Synpolydactyly type 2
Primary systemic amyloidosis

FBLN1
(UniProt - OMIM)
 APOA1
(UniProt - OMIM)

INTERACTOME
ASSOCIATIONS
(click on a score value to see the evidence)
FBLN1
(0.63)
APOA1


Citations in the biomedical literature:


Synpolydactyly type 2
FBLN1
Primary systemic amyloidosis
APOA1



Synpolydactyly type 2
Primary systemic amyloidosis

Synonym(s):
- SD2, Debeer type
- SD2b
- SPD, Debeer type
- SPD2
- Synpolydactyly, Debeer type
Synonym(s):
- Systemic AL amyloidosis
- Systemic immunoglobulinic amyloidosis
Classification (Orphanet):
- Rare bone disease
- Rare developmental defect during embryogenesis
- Rare genetic disease
Classification (Orphanet):
- Rare cardiac disease
- Rare genetic disease
- Rare hematologic disease
- Rare neurologic disease
- Rare oncologic disease
- Rare renal disease
- Rare systemic or rheumatologic disease
Classification (ICD10):
- Congenital malformations, deformations and chromosomal abnormalities -
Classification (ICD10):
- Endocrine, nutritional and metabolic diseases -
Epidemiological data:
(no data available)
Epidemiological data:
(no data available)
External references:
1 OMIM reference -
No MeSH references
External references:
1 OMIM reference -
No MeSH references
No signs/symptoms info available.