raremaprare-disease reference indexOrphadata 2026-06-23 · HPO 2026-09-01
ORPHA:238766

Ptosis-syndactyly-learning difficulties syndrome

inactive · moved to ORPHA:2841608q21.11 microdeletion 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 8q21.11 microdeletion syndrome

1

Names in Orphadata languages

12 of 12 languages
LangNameSynonyms
enPtosis-syndactyly-learning difficulties syndrome
frSyndrome de ptosis-syndactylie-difficultés d'apprentissage
dePtosis - Syndaktylie - Lernschwierigkeiten
esSíndrome de ptosis-sindactilia-dificultades de aprendizaje
itPtosi - sindattilia - difficoltà di apprendimento
nlPtose - syndactylie - leermoeilijkheden-syndroom
ptSíndrome de ptose-sindactilia-dificuldades de aprendizagem
plPtoza - syndaktylia - trudności w uczeniu się
csSyndrom zahrnující ptózu, syndaktylii a potíže s učením
ukСиндром птозу-синдактилії-труднощів у навчанні
zh上睑下垂-并指(趾)-学习障碍综合征
trPitozis-sindaktili-öğrenme zorlukları 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