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Infantile autosomal recessive medullary cystic kidney disease
4 associated genes
No signs/symptoms info
PROTEIN INTERACTIONS: 1
Multiple keratoacanthoma, Ferguson-Smith type
1 OMIM reference -
1 associated gene
No signs/symptoms info
Infantile autosomal recessive medullary cystic kidney disease
Multiple keratoacanthoma, Ferguson-Smith type

ANKS6
(UniProt - OMIM)
 TGFBR1
(UniProt - OMIM)
INVS
(UniProt - OMIM)
NEK8
(UniProt - OMIM)
TTC21B
(UniProt - OMIM)

INTERACTOME
ASSOCIATIONS
(click on a score value to see the evidence)
NEK8
(0.59)
TGFBR1


Citations in the biomedical literature:


Infantile autosomal recessive medullary cystic kidney disease
ANKS6 INVS NEK8 TTC21B
Multiple keratoacanthoma, Ferguson-Smith type
TGFBR1



Infantile autosomal recessive medullary cystic kidney disease
Multiple keratoacanthoma, Ferguson-Smith type

Synonym(s):
(no synonyms)

Synonym(s):
- ESS1
- MSSE
- Multiple self-healing squamous epithelioma
- Self-healing squamous epithelioma type 1
Classification (Orphanet):
- Rare genetic disease
- Rare renal disease
Classification (Orphanet):
- Rare eye disease
- Rare genetic disease
- Rare oncologic disease
- Rare skin disease
Classification (ICD10):
- Congenital malformations, deformations and chromosomal abnormalities -
Classification (ICD10):
- Neoplasms -
Epidemiological data:
(no data available)
Epidemiological data:
Class of prevalence: unknown
Average age onset: variable
Average age of death: normal
Type of inheritance: autosomal dominant
External references:
No OMIM references
No MeSH references
External references:
1 OMIM reference -
No MeSH references
No signs/symptoms info available.