raremaprare-disease reference indexOrphadata 2026-06-23 · HPO 2026-09-01
ORPHA:464764

Immune-mediated acquired neuromuscular junction disease

Type
Clinical group
Group
Group of disorders
Status
active

This term does not characterize a disease but a group of diseases. To learn about the diseases included under this term, you can consult the classifications.

1

Names in Orphadata languages

12 of 12 languages
LangNameSynonyms
enImmune-mediated acquired neuromuscular junction disease
frMaladie acquise de la jonction neuromusculaire à médiation immune
deImmun-vermittelte erworbene neuromuskuläre Übertragungsstörung
esEnfermedad de la unión neuromuscular adquirida mediada por el sistema inmunitario
itMalattia acquisita immuno-mediata della giunzione neuromuscolare
nlImmuungemedieerde verworven neuromusculaire junctiestoornisImmuungemedieerde verworven neuromusculaire transmissiestoornis · Immuungemedieerde verworven stoornis van de motorische eindplaat
ptDoença da junção neuromuscular adquirida imunomediada
plNabyta choroba połączeń nerwowo-mięśniowych o podłożu immunologicznym
csImunitně mediovaná získaná porucha nervosvalové ploténky
ukІмуноопосередкована набута хвороба нервово-мязових зєднань
zh免疫介导的获得性神经肌肉接头疾病
trBağışıklık aracılı edinsel nöromüsküler bağ hastalığı
2

Cross-references

qualifier = Orphanet mapping relation
SourceCodeQualifierICD relationValidation
MONDO18743Evalidated
UMLSC5681096Evalidated

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

3

Classification

Preferential parent (Orphanet linearisation):

Parents in the classifications (1):

Children (3):

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