raremaprare-disease reference indexOrphadata 2026-06-23 · HPO 2026-09-01
ORPHA:567556

Genetic systemic disease with glomerulopathy as a major feature

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
enGenetic systemic disease with glomerulopathy as a major feature
frMaladie systémique d'origine génétique avec une glomérulopathie comme manifestation majeure
deGenetisch bedingte systemische Krankheit mit Glomerulopathie als Hauptmerkmal
esEnfermedad sistémica genética con glomerulopatía como característica principal
itMalattia sistemica genetica a prevalente espressione glomerulopatica
nlGenetische systemische ziekte met glomerulopathie als hoofdkenmerk
ptGlomerulopatia como característica principal em doença sistémica genética
plGenetyczna choroba wieloukładowa z glomerulopatią jako głównym objawem
csGenetické systémové onemocnění s glomerulopatií jako hlavním příznakem
ukГенетично обумовлене системне захворювання з гломерулопатією як основною ознакою
zh以肾小球病变为主要特征的遗传性系统性疾病
trEsas klinik özelliği glomerülopati olan genetik sistemik hastalık
2

Cross-references

qualifier = Orphanet mapping relation
SourceCodeQualifierICD relationValidation
UMLSC5681295Evalidated

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):

Children (5):

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