Elig.phs001207.v3.p1.1
Item
Our AA sample collection was taken from an extensive cohort of AA sarcoidosis patients and family members from the sarcoidosis genetic analysis (SAGA) sample ascertained through affected sib pairs and a nuclear family-based sample ascertained through single sarcoidosis-affected offspring from the Henry Ford Health System in Detroit, Michigan. Subjects were considered as sarcoidosis cases if they met criteria for either definite or highly probable cases of sarcoidosis. Definite cases had noncaseating granulomas (histologically confirmed) and clinical manifestations in either the thorax or at least two other organs. Highly probable cases showed bilateral hilar adenopathy in their chest radiographs and either had a history of erythema nodosum or no other disease was diagnosed at least for 2 years observation to explain radiographic abnormalities. Cases with active tuberculosis were excluded. Unaffected family members were included in the study to serve as a control group.
boolean
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C0680063 (UMLS CUI [2,6])
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C0242801 (UMLS CUI [3,1])
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C0014743 (UMLS CUI [5,8])
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C0086282 (UMLS CUI [7,1])
C0522477 (UMLS CUI [7,2])
C1512693 (UMLS CUI [7,3])
C0009932 (UMLS CUI [7,4])