raremaprare-disease reference indexOrphadata 2026-06-23 · HPO 2026-09-01
ORPHA:98594

Rare eyebrow/eyelash disorder

Synonyms: Rare eyebrow/eyelashes anomaly

Type
Category
Group
Group of disorders
Status
active

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.

1

Names in Orphadata languages

12 of 12 languages
LangNameSynonyms
enRare eyebrow/eyelash disorderRare eyebrow/eyelashes anomaly
frAnomalies des cils ou des sourcils
deAugenbrauen/Augenwimpern-Anomalie, seltene
esAnomalía raras de las cejas y pestañas
itAnomalia rara delle sopracciglia-ciglia
nlZeldzame wenkbrauw/wimperanomalie
ptDoença das sobrancelhas/pestanas rara
plRzadka wada brwi/rzęs= en
csVzácné anomálie obočí/řas= en
ukРідкісний розлад брів/війРідкісна аномалія брів/вій
zh罕见眉/睫毛紊乱罕见眉/睫毛异常
trNadir kaş/kirpik bozukluğuNadir kaş/kirpik anomalisi
2

Cross-references

qualifier = Orphanet mapping relation
SourceCodeQualifierICD relationValidation
UMLSC5680326Evalidated

E exact · NTBT this ORPHAcode is narrower than the target · BTNT broader than the target · ND not decided.

3

Classification

Preferential parent (Orphanet linearisation):

Parents in the classifications (4):

Children (2):

Codes that Orphanet moved or referred to this one:

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