raremaprare-disease reference indexOrphadata 2026-06-23 · HPO 2026-09-01
ORPHA:101052

OBSOLETE: Microlissencephaly type B

inactive · referred to ORPHA:1083Microlissencephaly

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 Microlissencephaly

1

Names in Orphadata languages

12 of 12 languages
LangNameSynonyms
enOBSOLETE: Microlissencephaly type B
frOBSOLETE : Microlissencéphalie type B
deOBSOLET: Mikrolissenzephalie Typ B
esOBSOLETO: Microlisencefalia tipo B
itOBSOLETO: Microlissencefalia, tipo B
nlOBSOLEET: Microlissencefalie type B
ptOBSOLETO: Microlisencefalia, tipo B
plNIEAKTUALNE: Mikrolizencefalia typu B
csNEAKTUÁLNÍ: Mikrolissencefalie typu B
ukЗАСТАРІЛО: Мікролісенцефалія, тип В
zh弃用:小头畸形B型
trEski adı: Mikrolizensefali tip B
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