raremaprare-disease reference indexOrphadata 2026-06-23 · HPO 2026-09-01
ORPHA:399185

Rare hereditary disease with avascular necrosis

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 hereditary disease with avascular necrosis
frMaladie héréditaire rare avec nécrose avasculaire
deSeltene hereditäre Krankheit mit avaskulärer Nekrose
esEnfermedad hereditaria rara con necrosis avascular
itMalattia ereditaria rara con necrosi avascolare
nlZeldzame erfelijke ziekte met avasculaire necrose
ptDoença hereditária rara com necrose avascular
plRzadka choroba dziedziczna z martwicą awaskularną
csVzácná dědičná onemocnění s avaskulární nekrózou
ukРідкісне спадкове захворювання з аваскулярним некрозом
zh罕见遗传病伴缺血性坏死
trAvasküler nekroz ile seyreden nadir kalıtsal hastalık
2

Cross-references

qualifier = Orphanet mapping relation
SourceCodeQualifierICD relationValidation
MONDO18377Evalidated
UMLSC5681170Evalidated

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 (4):

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