Cytoscape Web
Click node...

Infantile autosomal recessive medullary cystic kidney disease
4 associated genes
No signs/symptoms info
COMMON GENES: 1
Renal-hepatic-pancreatic dysplasia
2 OMIM references -
2 associated genes
No signs/symptoms info
Infantile autosomal recessive medullary cystic kidney disease
Renal-hepatic-pancreatic dysplasia

ANKS6
(UniProt - OMIM)
 NEK8
(UniProt - OMIM)
INVS
(UniProt - OMIM)
 NPHP3
(UniProt - OMIM)
NEK8
(UniProt - OMIM)
TTC21B
(UniProt - OMIM)

COMMON
GENES 		NEK8


Citations in the biomedical literature:


Infantile autosomal recessive medullary cystic kidney disease
ANKS6 INVS NEK8 TTC21B
Renal-hepatic-pancreatic dysplasia
NPHP3



Infantile autosomal recessive medullary cystic kidney disease
Renal-hepatic-pancreatic dysplasia

Synonym(s):
(no synonyms)

Synonym(s):
- Ivemark II syndrome
- Renohepaticopancreatic dysplasia
Classification (Orphanet):
- Rare genetic disease
- Rare renal disease
Classification (Orphanet):
- Rare abdominal surgical disease
- Rare developmental defect during embryogenesis
- Rare genetic disease
- Rare renal disease
Classification (ICD10):
- Congenital malformations, deformations and chromosomal abnormalities -
Classification (ICD10):
(no data available)
Epidemiological data:
(no data available)
Epidemiological data:
(no data available)
External references:
No OMIM references
No MeSH references
External references:
2 OMIM references -
No MeSH references
No signs/symptoms info available.