ORPHA:723416

Genetic 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.

Names in Orphadata languages

9 of 12 languages

Lang	Name	Synonyms
en	Genetic arthrogryposis syndrome
fr	Syndrome arthrogrypose génétique
de	Genetisches Arthrogrypose-Syndrom
es	Síndrome de artrogriposis genética
it	Sindrome genetica da artrogriposi
nl	Genetisch artrogryposesyndroom
pt	Genetic arthrogryposis syndrome
pl	Genetic arthrogryposis syndrome
cs	Genetic arthrogryposis syndrome

Cross-references

qualifier = Orphanet mapping relation

No cross-references in this release.

Classification

Preferential parent (Orphanet linearisation):

ORPHA:93890Rare developmental defect during embryogenesis

Parents in the classifications (1):

ORPHA:404577Genetic syndrome with limb malformations as a major feature
rare genetic diseases

Children (6):

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/723416
This record as JSON: /data/d/723416.json