raremaprare-disease reference indexOrphadata 2026-06-23 · HPO 2026-09-01
ORPHA:306507

LAMB2-related infantile-onset nephrotic syndrome

inactive · moved to ORPHA:2670Pierson syndrome

Type
Disease
Group
Disorder
Status
inactive
Flag
Deprecated entity

This entity has been excluded from the Orphanet nomenclature of rare diseases and moved to Pierson syndrome

1

Names in Orphadata languages

12 of 12 languages
LangNameSynonyms
enLAMB2-related infantile-onset nephrotic syndrome
frSyndrome néphrotique infantile lié à LAMB2
deLAMB2-assoziiertes nephrotisches Syndrom mit Beginn im KindesalterNephrotisches Syndrom Typ 5
esSíndrome nefrótico asociado al gen LAMB2 de inicio en la infancia
itSindrome nefrosica correlata a LAMB2 ad esordio infantile
nlLAMB2-gerelateerd nefrotisch syndroom met infantiele aanvang
ptSíndrome nefrótico com início na infância LAMB-2-relacionado
plZespół nefrotyczny zwiazany z LAMB-2 o początku w wieku niemowlęcym
csLAMB2-vázaný nefrotický syndrom s nástupem v dětském věku
ukLAMB2-асоційований інфантильний нефротичний синдром
zhLAMB2基因相关婴儿肾病综合征
trLAMB2-ilişkili infantil başlangıçlı nefrotik sendrom
2

Cross-references

qualifier = Orphanet mapping relation
SourceCodeQualifierICD relationValidation
OMIM614199Evalidated

E exact · NTBT this ORPHAcode is narrower than the target · BTNT broader than the target · ND not decided.

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