loading...| Preferred Name | renal cysts and diabetes syndrome | |
| Synonyms |
glomerulocystic kidney disease, hypoplastic type glomerulocystic kidney, familial hypoplastic maturity-onset diabetes of the young type 5 FJHN atypical MODY type 5 maturity-onset diabetes of the Young, type 5 FJHN, atypical hyperuricemic nephropathy, familial juvenile, atypical HNF1B-MODY RCAD renal cysts and diabetes syndrome renal cysts-maturity-onset diabetes of the young syndrome RCAD syndrome atypical familial juvenile hyperuricemic nephropathy hepatocyte nuclear Factor 1-beta-associated monogenic diabetes hypoplastic type glomerulocystic kidney disease familial hypoplastic glomerulocystic kidney maturity onset diabetes of the Young, type 5 MODY5 atypical FJHN renal dysfunction-early-onset diabetes syndrome CAKUT with diabetes HNF1B-related renal cysts and diabetes syndrome congenital anomalies of the kidney and urinary tract with diabetes |
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| Definitions |
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. |
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| ID |
http://purl.obolibrary.org/obo/MONDO_0007669 |
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| altLabel |
glomerulocystic kidney disease, hypoplastic type glomerulocystic kidney, familial hypoplastic maturity-onset diabetes of the young type 5 FJHN atypical MODY type 5 maturity-onset diabetes of the Young, type 5 FJHN, atypical hyperuricemic nephropathy, familial juvenile, atypical HNF1B-MODY RCAD renal cysts and diabetes syndrome renal cysts-maturity-onset diabetes of the young syndrome RCAD syndrome atypical familial juvenile hyperuricemic nephropathy hepatocyte nuclear Factor 1-beta-associated monogenic diabetes hypoplastic type glomerulocystic kidney disease familial hypoplastic glomerulocystic kidney maturity onset diabetes of the Young, type 5 MODY5 atypical FJHN renal dysfunction-early-onset diabetes syndrome CAKUT with diabetes HNF1B-related renal cysts and diabetes syndrome congenital anomalies of the kidney and urinary tract with diabetes |
|
| definition |
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. |
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| has_exact_synonym |
HNF1B-MODY RCAD renal cysts and diabetes syndrome renal cysts-maturity-onset diabetes of the young syndrome RCAD syndrome atypical familial juvenile hyperuricemic nephropathy hepatocyte nuclear Factor 1-beta-associated monogenic diabetes hypoplastic type glomerulocystic kidney disease familial hypoplastic glomerulocystic kidney maturity onset diabetes of the Young, type 5 MODY5 atypical FJHN renal dysfunction-early-onset diabetes syndrome CAKUT with diabetes HNF1B-related renal cysts and diabetes syndrome congenital anomalies of the kidney and urinary tract with diabetes |
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| has_related_synonym |
glomerulocystic kidney disease, hypoplastic type glomerulocystic kidney, familial hypoplastic maturity-onset diabetes of the young type 5 FJHN atypical MODY type 5 maturity-onset diabetes of the Young, type 5 FJHN, atypical hyperuricemic nephropathy, familial juvenile, atypical |
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| label |
renal cysts and diabetes syndrome |
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| prefixIRI |
MONDO:0007669 |
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| prefLabel |
renal cysts and diabetes syndrome |
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| seeAlso |
https://rarediseases.info.nih.gov/diseases/10221/maturity-onset-diabetes-of-the-young-type-5 |
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| textual definition |
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. |
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| subClassOf |