raremaprare-disease reference indexOrphadata 2026-06-23 · HPO 2026-09-01
ORPHA:1680

OBSOLETE: Spastic diplegia, infantile type

inactive · referred to ORPHA:102003Rare movement disorder

Synonyms: OBSOLETE: Little syndrome

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 Rare movement disorder

1

Names in Orphadata languages

12 of 12 languages
LangNameSynonyms
enOBSOLETE: Spastic diplegia, infantile typeOBSOLETE: Little syndrome
frOBSOLETE : Diplégie spastique infantileOBSOLETE : Syndrome de Little
deOBSOLET: Infantile spastische DiplegieOBSOLET: Little-Syndrom
esOBSOLETO: Diplejía espástica tipo infantilOBSOLETO: Síndrome de Little
itOBSOLETO: Diplegia spastica, tipo infantileOBSOLETO: Sindrome di Little
nlOBSOLEET: Spastische diplegie, infantiel typeOBSOLEET: Syndroom van Little
ptOBSOLETO: Diplegia espástica, tipo infantilOBSOLETO: Síndrome Little
plNIEAKTUALNE: Obustronne porażenie kurczowe, postać niemowlęcaNIEAKTUALNE: Zespół Little'a
csNEAKTUÁLNÍ: Spastická diplegie, infantilní typNEAKTUÁLNÍ: Littleův syndrom
ukЗАСТАРІЛО: Спастична диплегія, інфантильний типЗАСТАРІЛО: Синдром Літтла
zh弃用:痉挛性双侧瘫痪,婴儿型Little综合征
trEski adı: Spastik dipleji, infantil tipKüçük sendrom
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