raremaprare-disease reference indexOrphadata 2026-06-23 · HPO 2026-09-01
ORPHA:98056

Rare genetic 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
LangNameSynonyms
enRare genetic renal disease
frMaladie rénale génétique rare
deNierenkrankheit, genetisch bedingte
esEnfermedades renales genéticas raras
itMalattia renale genetica rara
nlZeldzame genetische nierziekte
ptDoença genética renal
plRzadka uwarunkowana genetycznie choroba nerek
csVzácná geneticky podmíněná onemocnění ledvin
ukРідкісне генетично обумовлене захворювання нирок
zh罕见遗传性肾病
trNadir genetik böbrek hastalığı
2

Cross-references

qualifier = Orphanet mapping relation
SourceCodeQualifierICD relationValidation
UMLSC5681504Evalidated

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 (1):

Children (8):

4

Genes

0 direct

Orphanet records no gene directly on this code.

5

Prevalence and incidence

0 records

No prevalence record in this release.

6

HPO phenotypes

Orphanet has no HPO annotation for this code in this release.

7

Sources for this card