raremaprare-disease reference indexOrphadata 2026-06-23 · HPO 2026-09-01
ORPHA:399380

Osteonecrosis of genetic origin

Synonyms: Bone 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
enOsteonecrosis of genetic originBone necrosis of genetic origin
frOstéonécrose d'origine génétiqueNécrose osseuse d'origine génétique
deOsteonekrose, genetisch bedingteKnochennekrose genetischen Ursprungs
esOsteonecrosis de origen genéticoNecrosis ósea de origen genético
itOsteonecrosi di origine geneticaNecrosi ossea di origine genetica
nlOsteonecrose van genetische oorsprongBotnecrose van genetische oorsprong
ptOsteonecrose de origem genética
plOsteonekroza pochodzenia genetycznegoMartwica kości pochodzenia genetycznego
csOsteonekróza genetického původuNekróza kosti genetického původu
ukГенетично обумовлений остеонекрозНекроз кісток генетичного походження
zh遗传性骨坏死遗传性骨坏死
trGenetik kökenli osteonekrozGenetik kaynaklı kemik nekrozu
2

Cross-references

qualifier = Orphanet mapping relation
SourceCodeQualifierICD relationValidation
MONDO0018383Evalidated
MONDO18383Evalidated
UMLSC5680035Evalidated

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 (3):

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