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renal cysts and diabetes syndrome

The information provided on this page is for informational purposes only. The National Organization for Rare Disorders (NORD) does not endorse the information presented. The content has been gathered in partnership with the MONDO Disease Ontology. Please consult with a healthcare professional for medical advice and treatment.

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Disease Overview

Renal cysts and diabetes syndrome (RCAD) is a rare form of maturity-onset diabetes of the young (MODY) characterized clinically by heterogeneous cystic renal disease and early-onset familial non-autoimmune diabetes. Pancreatic atrophy, liver dysfunction and genital tract anomalies are also features of the syndrome.

Synonyms

  • CAKUT with diabetes
  • FJHN atypical
  • FJHN, atypical
  • HNF1B-MODY
  • HNF1B-related renal cysts and diabetes syndrome
  • MODY type 5
  • MODY5
  • RCAD
  • RCAD syndrome
  • atypical FJHN
  • atypical familial juvenile hyperuricemic nephropathy
  • congenital anomalies of the kidney and urinary tract with diabetes
  • familial hypoplastic glomerulocystic kidney
  • glomerulocystic kidney disease, hypoplastic type
  • glomerulocystic kidney, familial hypoplastic
  • hepatocyte nuclear Factor 1-beta-associated monogenic diabetes
  • hyperuricemic nephropathy, familial juvenile, atypical
  • hypoplastic type glomerulocystic kidney disease
  • maturity onset diabetes of the Young, type 5
  • maturity-onset diabetes of the Young, type 5
  • maturity-onset diabetes of the young type 5
  • renal cysts and diabetes syndrome
  • renal cysts-maturity-onset diabetes of the young syndrome
  • renal dysfunction-early-onset diabetes syndrome
GARD Disease Summary

The Genetic and Rare Diseases Information Center (GARD) has information and resources for patients, caregivers, and families that may be helpful before and after diagnosis of this condition. GARD is a program of the National Center for Advancing Translational Sciences (NCATS), part of the National Institutes of Health (NIH).

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Orphanet

Orphanet has a summary about this condition that may include information on the diagnosis, care, and treatment as well as other resources. Some of the information and resources are available in languages other than English. The summary may include medical terms, so we encourage you to share and discuss this information with your doctor. Orphanet is the French National Institute for Health and Medical Research and the Health Programme of the European Union.

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OMIM

Online Mendelian Inheritance In Man (OMIM) has a summary of published research about this condition and includes references from the medical literature. The summary contains medical and scientific terms, so we encourage you to share and discuss this information with your doctor. OMIM is authored and edited at the McKusick-Nathans Institute of Genetic Medicine, Johns Hopkins University School of Medicine.

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