Cytoscape Web
Click node...

Synpolydactyly type 2
1 OMIM reference -
1 associated gene
No signs/symptoms info
PROTEIN INTERACTIONS: 1
Benign paroxysmal torticollis of infancy
1 associated gene
No signs/symptoms info
Synpolydactyly type 2
Benign paroxysmal torticollis of infancy

FBLN1
(UniProt - OMIM)
 CACNA1A
(UniProt - OMIM)

INTERACTOME
ASSOCIATIONS
(click on a score value to see the evidence)
FBLN1
(0.63)
CACNA1A


Citations in the biomedical literature:


Synpolydactyly type 2
FBLN1
Benign paroxysmal torticollis of infancy
CACNA1A



Synpolydactyly type 2
Benign paroxysmal torticollis of infancy

Synonym(s):
- SD2, Debeer type
- SD2b
- SPD, Debeer type
- SPD2
- Synpolydactyly, Debeer type
Synonym(s):
(no synonyms)
Classification (Orphanet):
- Rare bone disease
- Rare developmental defect during embryogenesis
- Rare genetic disease
Classification (Orphanet):
- Rare genetic disease
- Rare neurologic disease
Classification (ICD10):
- Congenital malformations, deformations and chromosomal abnormalities -
Classification (ICD10):
- Diseases of the nervous system -
Epidemiological data:
(no data available)
Epidemiological data:
Class of prevalence: <1 / 1 000 000
Average age onset: childhood
Average age of death: normal
Type of inheritance: sporadic
External references:
1 OMIM reference -
No MeSH references
External references:
No OMIM references
No MeSH references
No signs/symptoms info available.