ORPHA:98750

Autoimmune neurological channelopathy

Type: Category
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.

Names in Orphadata languages

12 of 12 languages

Lang	Name	Synonyms
en	Autoimmune neurological channelopathy
fr	Canalopathie neurologique auto-immune
de	Ionenkanalkrankheit, autoimmune neurologische
es	Canalopatía neurológica autoinmune
it	Canalopatia neurologica autoimmune
nl	Auto-immune neurologische kanalopathie
pt	Canalopatia neurológica autoimune
pl	Autoimmunologiczna kanałopatia neurologiczna
cs	Autoimunitní neurologické kanálopatie
uk	Аутоімунна неврологічна каналопатія
zh	自身免疫性神经离子通道病
tr	Otoimmün nörolojik kanalopati

Cross-references

qualifier = Orphanet mapping relation

Source	Code	Qualifier	ICD relation	Validation
UMLS	C5681703	E		validated

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

Classification

Preferential parent (Orphanet linearisation):

ORPHA:98006Rare neurologic disease

Parents in the classifications (1):

ORPHA:71864Muscular channelopathy
rare neurological diseases

Children (4):

Codes that Orphanet moved or referred to this one:

ORPHA:98751OBSOLETE: Autoimmune neurological channelopathy due to a p/q-type voltage gated calcium channel defect referred to · inactive
ORPHA:98752OBSOLETE: Autoimmune neurological channelopathy due to a potassium channel defect referred to · inactive
ORPHA:98753OBSOLETE: Autoimmune neurological channelopathy due to an acetylcholine receptor subunits defect referred to · inactive

Genes

0 direct

Orphanet records no gene directly on this code.

Prevalence and incidence

0 records

No prevalence record in this release.

HPO phenotypes

Orphanet has no HPO annotation for this code in this release.

Sources for this card

Orphanet page: orpha.net/en/disease/detail/98750
This record as JSON: /data/d/98750.json