raremaprare-disease reference indexOrphadata 2026-06-23 · HPO 2026-09-01
ORPHA:3311

OBSOLETE: Infantile symmetrical thalamic degeneration

inactive · referred to ORPHA:1314Symmetrical thalamic calcifications

Type
Disease
Group
Disorder
Status
inactive
Flag
Obsolete entity

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

1

Names in Orphadata languages

12 of 12 languages
LangNameSynonyms
enOBSOLETE: Infantile symmetrical thalamic degeneration
frOBSOLETE : Dégénérescence thalamique symétrique infantile
deOBSOLET: Thalamusdegeneration, infantile symmetrischeOBSOLET: Thalamusdegeneration
esOBSOLETO: Degeneración talámica simétrica infantil
itOBSOLETO: Degenerazione talamica
nlOBSOLEET: Infantiele symmetrische thalamische degeneratie
ptOBSOLETO: Degenerescência talâmica simétrica da infância
plNIEAKTUALNE: Dzieciece symetryczne zwyrodnienie wzgórza
csNEAKTUÁLNÍ: Infantilní symetrická degenerace thalamu
ukЗАСТАРІЛО: Інфантильна симетрична дегенерація таламуса
zh弃用:婴儿对称性丘脑退行性变
trEski adı: İnfantil simetrik talamik dejenerasyon
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