Cytoscape Web
Click node...

SSR4-CDG
1 associated gene
No signs/symptoms info
PROTEIN INTERACTIONS: 1
Intermittent hydrarthrosis
2 associated genes
No signs/symptoms info
SSR4-CDG
Intermittent hydrarthrosis

SSR4
(UniProt - OMIM)
 MEFV
(UniProt - OMIM)
TNFRSF1A
(UniProt - OMIM)

INTERACTOME
ASSOCIATIONS
(click on a score value to see the evidence)
SSR4
(0.72)
TNFRSF1A


Citations in the biomedical literature:


SSR4-CDG
SSR4
Intermittent hydrarthrosis
MEFV TNFRSF1A



SSR4-CDG
Intermittent hydrarthrosis

Classification (Orphanet):
- Inborn errors of metabolism
- Rare developmental defect during embryogenesis
- Rare genetic disease
- Rare neurologic disease
Classification (Orphanet):
- Rare genetic disease
- Rare systemic or rheumatologic disease
Classification (ICD10):
- Endocrine, nutritional and metabolic diseases -
Classification (ICD10):
(no data available)
Epidemiological data:
Class of prevalence: <1 / 1 000 000
Average age onset: neonatal/infancy
Average age of death: -
Type of inheritance: x-linked recessive
Epidemiological data:
(no data available)
External references:
No OMIM references
No MeSH references
External references:
No OMIM references
No MeSH references
No signs/symptoms info available.