raremaprare-disease reference indexOrphadata 2026-06-23 · HPO 2026-09-01
ORPHA:399388

Avascular necrosis of genetic origin

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
enAvascular necrosis of genetic origin
frNécrose avasculaire d'origine génétique
deAvaskuläre Nekrose, genetisch bedingte
esNecrosis avascular de origen genético
itNecrosi avascolare di origine genetica
nlAvasculaire necrose van genetische oorsprong
ptNecrose avascular de origem genética
plMartwica awaskularna pochodzenia genetycznego
csAvaskulární nekróza genetického původu
ukГенетично обумовлений аваскулярний некроз
zh遗传性缺血性坏死
trGenetik kökenli avasküler nekroz
2

Cross-references

qualifier = Orphanet mapping relation
SourceCodeQualifierICD relationValidation
MONDO18384Evalidated
UMLSC5681169Evalidated

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 (2):

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