raremaprare-disease reference indexOrphadata 2026-06-23 · HPO 2026-09-01
ORPHA:2708

OBSOLETE: Oculocerebroosseous syndrome

inactive · referred to ORPHA:102283Multiple congenital anomalies/dysmorphic syndrome-intellectual disability

Synonyms: OBSOLETE: Plum 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 Multiple congenital anomalies/dysmorphic syndrome-intellectual disability

1

Names in Orphadata languages

12 of 12 languages
LangNameSynonyms
enOBSOLETE: Oculocerebroosseous syndromeOBSOLETE: Plum syndrome
frOBSOLETE : Syndrome oculo-cérébro-osseuxOBSOLETE : Syndrome de Plum
deOBSOLET: Okulo-zerebro-ossäres SyndromOBSOLET: Plum-Syndrom
esOBSOLETO: Síndrome óculo-cerebro-óseoOBSOLETO: Síndrome de Plum
itOBSOLETO: Sindrome oculo-cerebro-osseaOBSOLETO: Sindrome di Plum
nlOBSOLEET: Oculocerebro-ossaal syndroomOBSOLEET: Syndroom van Plum
ptOBSOLETO: Síndrome oculo-cerebro-ósseoOBSOLETO: Síndrome Plum
plNIEAKTUALNE: Zespól oczno-mózgowo-kostnyNIEAKTUALNE: Zspół pluma
csNEAKTUÁLNÍ: Okulocerebrooseální syndrom= en
ukЗАСТАРІЛО: Окулоцереброкістковий синдромЗАСТАРІЛО: Сливовий синдром
zh弃用:眼脑骨综合征Plum综合征
trEski adı: Oküloserebroosseous sendromuPlum 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