raremaprare-disease reference indexOrphadata 2026-06-23 · HPO 2026-09-01
ORPHA:101356

OBSOLETE: Lissencephaly-demyelinating axonal neuropathy syndrome

inactive · referred to ORPHA:102010Other syndrome with lissencephaly as a major feature

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 Other syndrome with lissencephaly as a major feature

1

Names in Orphadata languages

12 of 12 languages
LangNameSynonyms
enOBSOLETE: Lissencephaly-demyelinating axonal neuropathy syndrome
frOBSOLETE : Syndrome de lissencéphalie-neuropathie axonale démyélinisante
deOBSOLET: Lissenzephalie - demyelinisierende axonale Neuropathie
esOBSOLETO: Síndrome de lisencefalia-neuropatía desmielinizante axonal
itOBSOLETO: Lissencefalia - neuropatia assonale demielinizzante
nlOBSOLEET: Lissencefalie - demyeliniserende axonale neuropathie-syndroom
ptOBSOLETO: Lisencefalia - neuropatia axonal desmielinizante
plNIEAKTUALNE: Lizencefalia - demielinizacyjna neuropatia aksonalna
csNEAKTUÁLNÍ: Syndrom lissencefalie a demyelinizační axonální neuropatie
ukСиндром ліссенцефалії-демієлінізуючої аксональної нейропатії
zh弃用:无脑回-脱髓鞘性轴索神经病综合征
trEski adı: Lizensefali-demiyelinizan aksonal nöropati 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