raremaprare-disease reference indexOrphadata 2026-06-23 · HPO 2026-09-01
ORPHA:169349

Immuno-osseous dysplasia

Type
Clinical group
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
enImmuno-osseous dysplasia
frDysplasie immuno-osseuse
deDysplasie, immuno-ossäre
esDisplasia inmuno-ósea
itDisplasia immuno-ossea
nlImmuno-ossale dysplasie
ptDisplasia imuno-óssea
plDysplazja immunologiczno-szkieletowa
csImunooseální dysplázie
ukІмунно-кісткова дисплазія
zh免疫-骨发育不良
trİmmüno-osseöz displazi
2

Cross-references

qualifier = Orphanet mapping relation
SourceCodeQualifierICD relationValidation
ICD-114A01.32Especificvalidated
MONDO0015708Evalidated
MONDO15708Evalidated
UMLSC0432218Evalidated

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 (6):

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