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Autosomal dominant medullary cystic kidney disease with or without hyperuricemia
3 OMIM references -
2 associated genes
No signs/symptoms info
PROTEIN INTERACTIONS: 1
Autosomal recessive systemic lupus erythematosus
1 OMIM reference -
2 associated genes
No signs/symptoms info
Autosomal dominant medullary cystic kidney disease with or without hyperuricemia
Autosomal recessive systemic lupus erythematosus

MUC1
(UniProt - OMIM)
 DNASE1L3
(UniProt - OMIM)
UMOD
(UniProt - OMIM)
 PRKCD
(UniProt - OMIM)

INTERACTOME
ASSOCIATIONS
(click on a score value to see the evidence)
MUC1
(0.79)
PRKCD


Citations in the biomedical literature:


Autosomal dominant medullary cystic kidney disease with or without hyperuricemia
MUC1 UMOD
Autosomal recessive systemic lupus erythematosus
DNASE1L3 PRKCD



Autosomal dominant medullary cystic kidney disease with or without hyperuricemia
Autosomal recessive systemic lupus erythematosus

Synonym(s):
- Autosomal dominant nephronophthisis
Synonym(s):
- Autosomal recessive SLE
- Familial SLE
- Familial systemic lupus erythematosus
Classification (Orphanet):
(no data available)
Classification (Orphanet):
- Rare genetic disease
- Rare systemic or rheumatologic disease
Classification (ICD10):
- Congenital malformations, deformations and chromosomal abnormalities -
Classification (ICD10):
- Diseases of the musculoskeletal system and connective tissue -
Epidemiological data:
Class of prevalence: 1-9 / 1 000 000
Average age onset: adulthood
Average age of death: -
Type of inheritance: autosomal dominant
Epidemiological data:
Class of prevalence: <1 / 1 000 000
Average age onset: childhood
Average age of death: no data available
Type of inheritance: autosomal recessive
External references:
3 OMIM references -
No MeSH references
External references:
1 OMIM reference -
No MeSH references
No signs/symptoms info available.