raremaprare-disease reference indexOrphadata 2026-06-23 · HPO 2026-09-01
ORPHA:2621

OBSOLETE: Low birth weight-dwarfism-dysgammaglobulinemia syndrome

inactive · referred to ORPHA:101977Immunodeficiency due to predominantly antibodies defect

Synonyms: OBSOLETE: Christian-Rosenberg syndrome

Type
Malformation syndrome
Group
Disorder
Status
inactive
Flag
Obsolete entity

This entity has been obsoleted from the Orphanet nomenclature of rare diseases.<br/><br/>Instead, consider using Immunodeficiency predominantly affecting antibody production

1

Names in Orphadata languages

12 of 12 languages
LangNameSynonyms
enOBSOLETE: Low birth weight-dwarfism-dysgammaglobulinemia syndromeOBSOLETE: Christian-Rosenberg syndrome
frOBSOLETE : Syndrome de nanisme-dysgammaglobulinémieOBSOLETE : Syndrome de Christian-Rosenberg
deOBSOLET: Niedriges Geburtsgewicht-Kleinwuchs-Dysgammaglobulinämie-SyndromOBSOLET: Christian-Rosenberg-Syndrom
esOBSOLETO: Síndrome de bajo peso al nacer-talla baja significativa-disgammaglobulinemiaOBSOLETO: Síndrome de Christian-Rosenberg
itOBSOLETO: Sindrome basso peso alla nascita-nanismo-disgammaglobulinemiaOBSOLETO: Sindrome di Christian-Rosenberg
nlOBSOLEET: Laag geboortegewicht - dwerggroei - dysgammaglobulinemie-syndroomOBSOLEET: Syndroom van Christian-Rosenberg
ptOBSOLETO: Síndrome de baixo peso ao nascimento-nanismo-disgamaglobulinemiaOBSOLETO: Síndrome Christian-Rosenberg
plNIEAKTUALNE: Niska waga urodzeniowa - niski wzrost - dysgammaglobulinemiaNIEAKTUALNE: Zespół Christiana i Rosenberga
csNEAKTUÁLNÍ: Syndrom zahrnujícíc nízkou porodní hmotnost, zakrslost a dysgamaglobulinemii= en
ukСиндром низької маси тіла при народженні-карликовості-дисгаммаглобулінеміїЗАСТАРІЛО: Синдром Крістіана-Розенберга
zh弃用:低出生体重-矮小症-异常丙种球蛋白血综合征Christian-Rosenberg综合征
trEski adı: Düşük doğum ağırlığı-cücelik-disgamaglobülinemi sendromuChristian-Rosenberg 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