raremaprare-disease reference indexOrphadata 2026-06-23 · HPO 2026-09-01
ORPHA:1533

OBSOLETE: Craniosynostosis-fibular aplasia syndrome

inactive · referred to ORPHA:139393Syndromic craniosynostosis

Synonyms: OBSOLETE: Lowry syndrome

Type
Malformation syndrome
Group
Disorder
Status
inactive
Flag
Obsolete entity

This entity has been obsoleted from the Orphanet nomenclature of rare diseases.<br/><br/>Instead, consider using Syndromic craniosynostosis

1

Names in Orphadata languages

12 of 12 languages
LangNameSynonyms
enOBSOLETE: Craniosynostosis-fibular aplasia syndromeOBSOLETE: Lowry syndrome
frOBSOLETE : Syndrome de craniosynostose-aplasie du péronéOBSOLETE : Syndrome de Lowry
deOBSOLET: Kraniosynostose -Fibulaaplasie-SyndromOBSOLET: Lowry-Syndrom
esOBSOLETO: Síndrome de craneosinostosis-aplasia de peronéOBSOLETO: Síndrome de Lowry
itOBSOLETO: Craniosinostosi-aplasia del peroneOBSOLETO: Sindrome di Lowry
nlOBSOLEET: Craniosynostose - aplasie van fibula-syndroomOBSOLEET: Syndroom van Lowry
ptOBSOLETO: Síndrome de craniossinostose-aplasia da fíbulaOBSOLETO: Síndrome Lowry
plNIEAKTUALNE: Kraniosynostoza - aplazja kości strzałkowejNIEAKTUALNE: Zespół Lowry'ego
csNEAKTUÁLNÍ: Syndrom zahrnující kraniosynostózu a aplázii fibulyNEAKTUÁLNÍ: Lowryho syndrom
ukЗАСТАРІЛО: Синдром краніосиностозу-фібулярної аплазіїЗАСТАРІЛО: Синдром Лоурі
zh颅缝早闭-腓骨发育不良综合征Lowry综合征
trKraniyosinostoz-fibular aplazi sendromuLowry 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