raremaprare-disease reference indexOrphadata 2026-06-23 · HPO 2026-09-01
ORPHA:658810

Atrophoderma of Pasini and Pierini

Type
Disease
Group
Disorder
Inheritance
Unknown
Age of onset
Adult
Status
active

Orphadata ships no English definition for this code.

1

Names in Orphadata languages

10 of 12 languages
LangNameSynonyms
enAtrophoderma of Pasini and Pierini
frAtrophodermie de Pierini et Pasini
deAtrophodermie von Pasini und Pierini
esAtrofodermia de Pasini y Pierini
itAtrofodermia di Pasini e Pierini
nlAtrofodermie van Pasini en PieriniAtrophoderma van Pasini en Pierini
ptAtrofodermia Pasini e Pierini
plAtrofoderma Pasiniego i Pieriniego
csAtrofodermie Pasiniho a Pieriniho
ukАтрофодермія Пасіні та Пєріні
2

Cross-references

qualifier = Orphanet mapping relation
SourceCodeQualifierICD relationValidation
ICD-10L90.3Especificvalidated
ICD-11EE7YNTBTindexvalidated
MONDO0022513Evalidated
MONDO22513Evalidated
UMLSC3887897Evalidated
MedDRA10066406Evalidated

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):

No children.

4

Genes

0 direct

Orphanet records no gene directly on this code.

5

Prevalence and incidence

2 records
TypeClassValueAreaQualificationValidationSource
Cases/families100 casesWorldwideCase(s)Validated30085611[PMID]
Point prevalence<1 / 1 000 000—WorldwideClass onlyValidated30085611[PMID]_ORPHANET

Value is Orphadata's ValMoy: the mean estimate per 100 000 for prevalence and incidence, the number of cases or families for case reports.

6

HPO phenotypes

Orphanet has no HPO annotation for this code in this release.

7

Sources for this card