raremaprare-disease reference indexOrphadata 2026-06-23 · HPO 2026-09-01
ORPHA:1115

OBSOLETE: Recessive aplasia cutis congenita of limbs

inactive · referred to ORPHA:1114Aplasia cutis congenita

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 Aplasia cutis congenita

1

Names in Orphadata languages

12 of 12 languages
LangNameSynonyms
enOBSOLETE: Recessive aplasia cutis congenita of limbs
frOBSOLETE : Aplasie cutanée congénitale des membres autosomique récessive
deOBSOLET: Aplasia cutis congenita der Gliedmaßen, rezessive
esOBSOLETO: Aplasia cutis congénita de las extremidades forma recesiva
itOBSOLETO: Aplasia cutanea congenita degli arti, forma recessiva
nlOBSOLEET: Recessieve aplasia cutis congenita van ledematen
ptOBSOLETO: Aplasia cutânea congénita nos membros recessiva
plNIEAKTUALNE: Recesywny wrodzony ubytek skóry konczyn
csNEAKTUÁLNÍ: Recesivní aplasia cutis congenita končetin
ukЗАСТАРІЛО: Рецесивна вроджена аплазія шкірного покриву кінцівок
zh弃用:肢体隐性先天性表皮发育不良
trEski adı: Ekstremitelerde resesif aplasi cutis konjenita
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