raremaprare-disease reference indexOrphadata 2026-06-23 · HPO 2026-09-01
ORPHA:183447

Genetic epidermal appendage 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
enGenetic epidermal appendage anomaly
frAnomalie génétique des phanères
deAnomalien der Hautanhangsgebilde, genetisch bedingte
esAnomalía genética de los apéndices epidérmicos
itAnomalia delle appendici epidermiche di origine genetica
nlGenetisch epidermaal aanhangsel-anomalie
ptAnomalia genética dos apêndices epidérmicos
plWada wytworów naskórka uwarunkowana genetycznie
csGeneticky podmíněné anomálie kožních adnex
ukГенетично обумовлена аномалія придатків епідермісу
zh遗传性皮肤附属器异常
trGenetik epidermal apendaj anomalisi
2

Cross-references

qualifier = Orphanet mapping relation
SourceCodeQualifierICD relationValidation
UMLSC5680583Evalidated

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 (1):

Children (5):

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