ORPHA:93587
Genetic cystic renal disease
Synonyms: Hereditary cystic renal disease
- Type
- Category
- Group
- Group of disorders
- Status
- active
This term does not characterize a disease but a group of diseases. To learn about the diseases included under this term, you can consult the classifications.
1
Names in Orphadata languages
12 of 12 languages| Lang | Name | Synonyms |
|---|---|---|
| en | Genetic cystic renal disease | Hereditary cystic renal disease |
| fr | Maladie kystique rénale d'origine génétique | Maladie kystique rénale héréditaire |
| de | Zystische Nierenerkrankung, genetisch bedingte | Nierenkrankheit, zystische, hereditäre |
| es | Enfermedad renal quística genética | Enfermedad renal quística hereditaria |
| it | Malattia renale cistica genetica | Malattia cistica renale di natura genetica |
| nl | Genetische cystische nierziekte | Hereditaire cystische nierziekte |
| pt | Doença renal quística genética | Doença renal quística hereditária |
| pl | Rodzinna torbielowatość nerek | Genetycznie uwarunkowana torbielowatość nerek |
| cs | Geneticky podmíněná cystická onemocnění ledvin | = en |
| uk | Генетично обумовлене кістозне захворювання нирок | Спадкове кістозне захворювання нирок |
| zh | 家族性囊性肾病 | |
| tr | Ailesel kistik böbrek hastalığı |
2
Cross-references
qualifier = Orphanet mapping relation| Source | Code | Qualifier | ICD relation | Validation |
|---|---|---|---|---|
| UMLS | C5680285 | E | validated |
E exact · NTBT this ORPHAcode is narrower than the target · BTNT broader than the target · ND not decided.
3
Classification
Preferential parent (Orphanet linearisation):
Parents in the classifications (2):
- ORPHA:98056Rare genetic renal disease
rare genetic diseases - ORPHA:93626Rare renal disease
rare renal diseases
Children (24):
- ORPHA:2666Adult familial nephronophthisis-spastic quadriparesia syndrome
- ORPHA:730Autosomal dominant polycystic kidney disease
- ORPHA:88924Autosomal dominant polycystic kidney disease type 1 with tuberous sclerosis
- ORPHA:34149Autosomal dominant tubulointerstitial kidney disease
- ORPHA:731Autosomal recessive polycystic kidney disease
- ORPHA:110Bardet-Biedl syndrome
- ORPHA:1515Cranioectodermal dysplasia
- ORPHA:289Ellis-Van Creveld syndrome
- ORPHA:2031Hepatic fibrosis-renal cysts-intellectual disability syndrome
- ORPHA:726824Hepatorenocardiac degenerative fibrosis
- ORPHA:2318Joubert syndrome with oculorenal defect
- ORPHA:220497Joubert syndrome with renal defect
- ORPHA:401996Karyomegalic interstitial nephritis
- ORPHA:564Meckel syndrome
- ORPHA:79118Neonatal diabetes-congenital hypothyroidism-congenital glaucoma-hepatic fibrosis-polycystic kidneys syndrome
- ORPHA:655Nephronophthisis
- ORPHA:140976RHYNS syndrome
- ORPHA:294415Renal-hepatic-pancreatic dysplasia
- ORPHA:140969Saldino-Mainzer syndrome
- ORPHA:84081Senior-Boichis syndrome
- ORPHA:3156Senior-Loken syndrome
- ORPHA:805Tuberous sclerosis complex
- ORPHA:443988Ventriculomegaly-cystic kidney disease
- ORPHA:892Von Hippel-Lindau disease
4
Genes
0 directOrphanet records no gene directly on this code.
5
Prevalence and incidence
0 recordsNo prevalence record in this release.
6
HPO phenotypes
Orphanet has no HPO annotation for this code in this release.
7
Sources for this card
- Orphanet page: orpha.net/en/disease/detail/93587
- This record as JSON: /data/d/93587.json