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Intermittent hydrarthrosis
2 associated genes
No signs/symptoms info
PROTEIN INTERACTIONS: 1
Congenital fibrosis of extraocular muscles
6 OMIM references -
4 associated genes
No signs/symptoms info
Intermittent hydrarthrosis
Congenital fibrosis of extraocular muscles

MEFV
(UniProt - OMIM)
 KIF21A
(UniProt - OMIM)
TNFRSF1A
(UniProt - OMIM)
 PHOX2A
(UniProt - OMIM)
TUBB2B
(UniProt - OMIM)
TUBB3
(UniProt - OMIM)

INTERACTOME
ASSOCIATIONS
(click on a score value to see the evidence)
TNFRSF1A
(0.72)
TUBB2B


Citations in the biomedical literature:


Intermittent hydrarthrosis
MEFV TNFRSF1A
Congenital fibrosis of extraocular muscles
KIF21A PHOX2A TUBB2B TUBB3



Intermittent hydrarthrosis
Congenital fibrosis of extraocular muscles

Synonym(s):
(no synonyms)

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