{"orpha":207098,"name":"Qualitative or quantitative defects of integrin alpha-7","type":"Category","group":"Group of disorders","status":"active","flags":[],"synonyms":["Integrinopathy"],"definition":null,"note":"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.","url":"https://raremap.alftech.space/d/ORPHA-207098/","orphanet_url":"https://www.orpha.net/en/disease/detail/207098","names":{"fr":{"name":"Anomalie qualitative ou quantitative de l'intégrine alpha 7","synonyms":["Intégrinopathie"]},"de":{"name":"Integrin alpha-7, qualitative oder quantitative Defekte"},"es":{"name":"Defectos cualitativos o cuantitativos de la integrina alfa-7","synonyms":["Integrinopatía"]},"it":{"name":"Deficit qualitativi o quantitativi di integrina alfa-7"},"nl":{"name":"Kwalitatieve of kwantitatieve defecten van integrine alfa-7","synonyms":["Integrinopathie"]},"pt":{"name":"Deficiências qualitativas ou quantitativas da integrina alfa-7"},"pl":{"name":"Defekty jakościowe lub ilościowe integryny alfa-7","synonyms":["Integrynopatia"]},"cs":{"name":"Kvalitativní nebo kvantitativní defekty integrinu alfa-7","synonyms":["Integrinopatie"]},"uk":{"name":"Якісні або кількісні дефекти інтегрину альфа-7","synonyms":["Інтегринопатія"]},"zh":{"name":"整合素α-7的定性或定量缺陷","synonyms":["整合素病"]},"tr":{"name":"İntegrin alfa-7'nin kalitatif veya kantitatif defektleri","synonyms":["İntegrinopati"]}},"xrefs":[{"source":"MONDO","code":"16150","qualifier":"E","icd_relation":null,"validated":true},{"source":"UMLS","code":"C5679789","qualifier":"E","icd_relation":null,"validated":true}],"associations":[],"incoming_associations":[],"preferential_parent":{"orpha":98006,"name":"Rare neurologic disease"},"parents":[{"orpha":207049,"name":"Qualitative or quantitative protein defects in neuromuscular diseases","classifications":[156]}],"children":[{"orpha":34520,"name":"Congenital muscular dystrophy with integrin alpha-7 deficiency","type":"Disease"}],"genes":[],"genes_via_subtypes":[],"inheritance":[],"onset":[],"prevalence":[],"phenotypes":null}