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Muscle filaminopathy
1 OMIM reference -
1 associated gene
No signs/symptoms info
PROTEIN INTERACTIONS: 1
Juvenile autosomal recessive medullary cystic kidney disease
5 associated genes
No signs/symptoms info
Muscle filaminopathy
Juvenile autosomal recessive medullary cystic kidney disease

FLNC
(UniProt - OMIM)
 ANKS6
(UniProt - OMIM)
GLIS2
(UniProt - OMIM)
NPHP1
(UniProt - OMIM)
NPHP4
(UniProt - OMIM)
WDR19
(UniProt - OMIM)

INTERACTOME
ASSOCIATIONS
(click on a score value to see the evidence)
FLNC
(0.77)
NPHP1


Citations in the biomedical literature:


Muscle filaminopathy
FLNC
Juvenile autosomal recessive medullary cystic kidney disease
ANKS6 GLIS2 NPHP1 NPHP4 WDR19



Muscle filaminopathy
Juvenile autosomal recessive medullary cystic kidney disease

Classification (Orphanet):
- Rare genetic disease
- Rare neurologic disease
Classification (Orphanet):
- Rare genetic disease
- Rare renal disease
Classification (ICD10):
- Diseases of the nervous system -
Classification (ICD10):
- Congenital malformations, deformations and chromosomal abnormalities -
Epidemiological data:
(no data available)
Epidemiological data:
Class of prevalence: -
Average age onset: -
Average age of death: -
Type of inheritance: autosomal recessive
External references:
1 OMIM reference -
No MeSH references
External references:
No OMIM references
No MeSH references
No signs/symptoms info available.