Cytoscape Web
Click node...

Congenital fibrosis of extraocular muscles
6 OMIM references -
4 associated genes
No signs/symptoms info
PROTEIN INTERACTIONS: 1
Familial congenital palsy of trochlear nerve
1 OMIM reference -
1 associated gene
No signs/symptoms info
Congenital fibrosis of extraocular muscles
Familial congenital palsy of trochlear nerve

KIF21A
(UniProt - OMIM)
 KANK1
(UniProt - OMIM)
PHOX2A
(UniProt - OMIM)
TUBB2B
(UniProt - OMIM)
TUBB3
(UniProt - OMIM)

INTERACTOME
ASSOCIATIONS
(click on a score value to see the evidence)
KIF21A
(0.75)
KANK1


Citations in the biomedical literature:


Congenital fibrosis of extraocular muscles
KIF21A PHOX2A TUBB2B TUBB3
Familial congenital palsy of trochlear nerve
KANK1



Congenital fibrosis of extraocular muscles
Familial congenital palsy of trochlear nerve

Synonym(s):
- FEOM
Synonym(s):
(no synonyms)
Classification (Orphanet):
- Rare eye disease
- Rare genetic disease
- Rare neurologic disease
Classification (Orphanet):
- Rare eye disease
- Rare genetic disease
Classification (ICD10):
- Diseases of the eye and adnexa -
Classification (ICD10):
- Diseases of the eye and adnexa -
Epidemiological data:
Class of prevalence: -
Average age onset: -
Average age of death: -
Type of inheritance: autosomal dominant
Epidemiological data:
(no data available)
External references:
6 OMIM references -
No MeSH references
External references:
1 OMIM reference -
No MeSH references
No signs/symptoms info available.