raremaprare-disease reference indexOrphadata 2026-06-23 · HPO 2026-09-01
ORPHA:207098

Qualitative or quantitative defects of integrin alpha-7

Synonyms: Integrinopathy

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
enQualitative or quantitative defects of integrin alpha-7Integrinopathy
frAnomalie qualitative ou quantitative de l'intégrine alpha 7Intégrinopathie
deIntegrin alpha-7, qualitative oder quantitative Defekte
esDefectos cualitativos o cuantitativos de la integrina alfa-7Integrinopatía
itDeficit qualitativi o quantitativi di integrina alfa-7
nlKwalitatieve of kwantitatieve defecten van integrine alfa-7Integrinopathie
ptDeficiências qualitativas ou quantitativas da integrina alfa-7
plDefekty jakościowe lub ilościowe integryny alfa-7Integrynopatia
csKvalitativní nebo kvantitativní defekty integrinu alfa-7Integrinopatie
ukЯкісні або кількісні дефекти інтегрину альфа-7Інтегринопатія
zh整合素α-7的定性或定量缺陷整合素病
trİntegrin alfa-7'nin kalitatif veya kantitatif defektleriİntegrinopati
2

Cross-references

qualifier = Orphanet mapping relation
SourceCodeQualifierICD relationValidation
MONDO16150Evalidated
UMLSC5679789Evalidated

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 (1):

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