raremaprare-disease reference indexOrphadata 2026-06-23 · HPO 2026-09-01
ORPHA:90345

OBSOLETE: Unclassified metaphyseal chondrodysplasia

inactive · referred to ORPHA:93430Multiple metaphyseal dysplasia

Type
Disease
Group
Disorder
Status
inactive
Flag
Obsolete entity

This entity has been obsoleted from the Orphanet nomenclature of rare diseases.<br/><br/>Instead, consider using Multiple metaphyseal dysplasia

1

Names in Orphadata languages

12 of 12 languages
LangNameSynonyms
enOBSOLETE: Unclassified metaphyseal chondrodysplasia
frOBSOLETE : Chondrodysplasie métaphysaire non-classifiée
deOBSOLET: Chondrodysplasie, metaphysäre, weitere Formen
esOBSOLETO: Condrodisplasia metafisaria no clasificada
itOBSOLETO: Condrodisplasia metafisaria non classificata
nlOBSOLEET: Niet-geclassifceerde metafysaire chondrodysplasie
ptOBSOLETO: Condrodisplasia metafisária, outras
plNIEAKTUALNE: Niesklasyfikowana chondrodysplazja przenasadowa
csNEAKTUÁLNÍ: Neklasifikovaná metafyzární chondrodysplázie
ukЗАСТАРІЛО: Некласифікована метафізарна хондродисплазія
zh弃用:未分型干骺端软骨发育异常
trEski adı: Sınıflandırılmamış metafizer kondrodisplazi
2

Cross-references

qualifier = Orphanet mapping relation

No cross-references in this release.

3

Classification

Not placed in any Orphanet classification in this release.

No children.

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