raremaprare-disease reference indexOrphadata 2026-06-23 · HPO 2026-09-01
ORPHA:2431

Central bilateral macrogyria

inactive · moved to ORPHA:98889Bilateral perisylvian polymicrogyria

Type
Disease
Group
Disorder
Status
inactive
Flag
Deprecated entity

This entity has been excluded from the Orphanet nomenclature of rare diseases and moved to Bilateral perisylvian polymicrogyria

1

Names in Orphadata languages

12 of 12 languages
LangNameSynonyms
enCentral bilateral macrogyria
frMacrogyrie centrale bilatérale
deMakrogyrie, bilaterale zentrale
esMacrogiria central bilateral
itMacrogiria bilaterale centrale
nlCentrale bilaterale macrogyrie
ptMacrogiria central bilateral
plOśrodkowa obustronna makrogyria
csCentrální bilaterální makrogyrie
ukЦентральна двостороння макрогірія
zh双侧中央巨脑回
trSantral bilateral makrogria
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