raremaprare-disease reference indexOrphadata 2026-06-23 · HPO 2026-09-01
ORPHA:109007

Arthrogryposis syndrome

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
enArthrogryposis syndrome
frArthrogrypose
deArthrogrypose-Syndrom
esSíndrome de artrogriposis
itSindrome da artrogriposi
nlArtrogryposesyndroom
ptSíndrome de artrogripose
plZespół artrogrypozy
csArtrogrypózy
ukСиндром артрогрипозу
zh关节弯曲综合征
trArtrogripoz sendromu
2

Cross-references

qualifier = Orphanet mapping relation
SourceCodeQualifierICD relationValidation
ICD-11LD26.4Especificvalidated
MONDO0015225Evalidated
MONDO15225Evalidated
MeSHD001176Evalidated
UMLSC0003886Evalidated
GARD19870Evalidated

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 (8):

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