raremaprare-disease reference indexOrphadata 2026-06-23 · HPO 2026-09-01
ORPHA:434786

Rare genetic autonomic nervous system disorder

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.

1

Names in Orphadata languages

12 of 12 languages
LangNameSynonyms
enRare genetic autonomic nervous system disorder
frMaladie génétique rare du système nerveux autonome
deSeltene genetische Krankheit des autonomen Nervensystems
esTrastorno genético raro del sistema nervioso autónomo
itMalattia genetica rara del sistema nervoso autonomo
nlZeldzame genetische aandoening van autonoom zenuwstelsel
ptDoença genética do sistema nervoso autónomo
plRzadkie zaburzenia autonomicznego układu nerwowego uwarunkowane genetycznie
csVzácná genetická porucha autonomního nervového systému
ukРідкісний генетично обумовлений розлад вегетативної нервової системи
zh罕见的遗传性植物神经系统疾病
trNadir genetik otonom sinir sistemi bozukluğu
2

Cross-references

qualifier = Orphanet mapping relation
SourceCodeQualifierICD relationValidation
MONDO18557Evalidated
UMLSC5681212Evalidated

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 (4):

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