raremaprare-disease reference indexOrphadata 2026-06-23 · HPO 2026-09-01
ORPHA:79458

Oley syndrome

inactive · moved to ORPHA:113Bazex-Dupré-Christol syndrome

Synonyms: Congenital hypotrichosis-milia syndrome

Type
Malformation syndrome
Group
Disorder
Status
inactive
Flag
Deprecated entity

This entity has been excluded from the Orphanet nomenclature of rare diseases and moved to Bazex-Dupré-Christol syndrome

1

Names in Orphadata languages

12 of 12 languages
LangNameSynonyms
enOley syndromeCongenital hypotrichosis-milia syndrome
frSyndrome d'OleySyndrome d'hypotrichose congénitale-milia
deOley-SyndromKongenitale Hypotrichose - Milien
esSíndrome de OleyHipotricosis congénita-milia
itSindrome di OleyIpotricosi congenita - milia
nlSyndroom van OleyCongenitale hypotrichose - milia-syndroom
ptSíndrome OleyHipotricose-congénita-mília
plZespół Oley'aWrodzona hipotrichoza - prosaki
csOleyové syndromSyndrom zahrnující vrozenou hypotrichózu a milia
ukСиндром ОліСиндром вродженого гіпотрихозу-мілії
zhOley综合征先天性少毛-粟粒疹综合征
trOley sendromuDoğumsal hipotrikoz-milia sendromu
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