raremaprare-disease reference indexOrphadata 2026-06-23 · HPO 2026-09-01
ORPHA:295221

OBSOLETE: Madelung deformity, unilateral

inactive · referred to ORPHA:240Léri-Weill dyschondrosteosis

Type
Clinical subtype
Group
Subtype of disorder
Status
inactive
Flag
Obsolete entity

This entity has been obsoleted from the Orphanet nomenclature of rare diseases.<br/><br/>Instead, consider using Léri-Weill dyschondrosteosis

1

Names in Orphadata languages

12 of 12 languages
LangNameSynonyms
enOBSOLETE: Madelung deformity, unilateral
frOBSOLETE : Déformation de Madelung unilatéraleOBSOLETE : Maladie de Madelung unilatérale
deOBSOLET: Madelung-Deformität, unilateral
esOBSOLETO: Deformidad de Madelung unilateral
itOBSOLETO: Defomità di Madelung unilaterale
nlOBSOLEET: Madelung-deformiteit, unilateraalOBSOLEET: Unilaterale misvorming van Madelung
ptOBSOLETO: Deformidade de Madelung, unilateral
plNIEAKTUALNE: Deformacja Madelunga, jednostronna
csNEAKTUÁLNÍ: Madelungova deformita, unilaterální
ukЗАСТАРІЛО: Деформація Маделунга, одностороння
zh弃用:单侧Madelung畸形
trEski adı: Madelung deformitesi, unilateral
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