raremaprare-disease reference indexOrphadata 2026-06-23 · HPO 2026-09-01
ORPHA:93313

OBSOLETE: Multiple epiphyseal dysplasia, unclassified type

inactive · referred to ORPHA:251Multiple epiphyseal 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 epiphyseal dysplasia

1

Names in Orphadata languages

12 of 12 languages
LangNameSynonyms
enOBSOLETE: Multiple epiphyseal dysplasia, unclassified type
frOBSOLETE : Dysplasie épiphysaire multiple non classifiée
deOBSOLET: Dysplasie, epiphysäre multiple (weitere Typen)
esOBSOLETO: Displasia epifisaria múltiple no clasificada
itOBSOLETO: Displasia epifisaria multipla, altri tipi
nlOBSOLEET: Meervoudige epifysaire dysplasie, niet-geclassificeerd type
ptOBSOLETO: Displasia epifisária múltipla, outro tipo
plNIEAKTUALNE: Dysplazja wielonasadowa, typ niesklasyfikowany
csNEAKTUÁLNÍ: Mnohočetná epifyzární dysplázie, neklasifikovaný typ
ukЗАСТАРІЛО: Множинна епіфізарна дисплазія, некласифікований тип
zh弃用:多发性骨骺发育不良,未分类型
trEski adı: Multiple epifizyal displazi, sınıflandırılmamış tip
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