raremaprare-disease reference indexOrphadata 2026-06-23 · HPO 2026-09-01
ORPHA:98601

OBSOLETE: Eyebrow/eyelashes pigmentation anomaly

inactive · referred to ORPHA:98594Rare eyebrow/eyelash disorder

Type
Category
Group
Group of disorders
Status
inactive
Flag
Obsolete entity

This entity has been obsoleted from the Orphanet nomenclature of rare diseases.<br/><br/>This term does not characterize a disease but a group of diseases. To learn about the diseases included under this term, you can consult the classifications.<br/><br/>Instead, consider using Rare eyebrow/eyelash disorder

1

Names in Orphadata languages

12 of 12 languages
LangNameSynonyms
enOBSOLETE: Eyebrow/eyelashes pigmentation anomaly
frOBSOLETE : Anomalie de la pigmentation des cils ou des sourcils
deOBSOLET: Augenbrauen und Augenwimpern, Pigmentanomalie der
esOBSOLETO: Anomalías de la pigmentación de cejas/pestañas
itOBSOLETO: Pigmentazione anomala delle sopracciglia e ciglia
nlOBSOLEET: Pigmentatie-anomalie van wenkbrauw/wimper
ptOBSOLETO: Anomalia da pigmentação das sobrancelhas/pestanas
plNIEAKTUALNE: Zaburzenie pigmentacji brwi/rzes
csNEAKTUÁLNÍ: Anomálie pigmentace obočí/řas
ukЗАСТАРІЛО: Аномалія пігментації брів/вій
zh弃用:眉/睫毛色素沉着异常
trEski adı: Kaş/kirpik pigmentasyon anomalisi
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