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

FAN1
(UniProt - OMIM)
 NEK8
(UniProt - OMIM)
NPHP3
(UniProt - OMIM)
 NPHP3
(UniProt - OMIM)
XPNPEP3
(UniProt - OMIM)

COMMON
GENES 		NPHP3


Citations in the biomedical literature:


Late-onset autosomal recessive medullary cystic kidney disease
FAN1 NPHP3 XPNPEP3
Renal-hepatic-pancreatic dysplasia
NEK8



Late-onset 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:
Class of prevalence: -
Average age onset: -
Average age of death: -
Type of inheritance: autosomal recessive
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.