PMID | Allele | Disease | Population | Drug Names | SNP | Class | Sentence |
---|---|---|---|---|---|---|---|
6623449 | HLA (HLA) | congenital hypothyroidism | NA | NA | NA | unclassified | |
hla antigens and congenital hypothyroidism. | |||||||
6623449 | HLA (HLA) | congenital hypothyroidism | NA | NA | NA | unclassified | |
hla antigens a and b were determined in a group of 41 patients with congenital hypothyroidism and 36 of their mothers. | |||||||
7071815 | HLA (HLA) | congenital hypothyroidism | NA | NA | NA | unclassified | |
congenital hypothyroidism and hla. | |||||||
7071815 | HLA-A (HLA-A) | congenital hypothyroidism | NA | NA | NA | unclassified | |
hla-a, b and c antigens tested in 97 patients treated for congenital hypothyroidism, and in members of their families, are compared with normal frequencies from 635 controls. | |||||||
7071815 | HLA (HLA) | congenital hypothyroidism | NA | NA | NA | unclassified | |
congenital hypothyroidism thus appears to show a different relationship with hla from other thyroid disorders. | |||||||
6587656 | HLA-A (HLA-A) | peyronie disease | NA | NA | NA | unclassified | |
hla-a and b antigens in patients with peyronie disease. | |||||||
6587656 | HLA-A (HLA-A) | peyronie disease | NA | NA | NA | unclassified | |
using microdroplet lymphocyte cytotoxicity test, as a method of hla typing, 9 patients with peyronie disease were studied from a viewpoint of relationship between this disease and hla-a and b antigens. | |||||||
6588752 | HLA-B*08 | schmidt syndrome | NA | insulin | NA | unclassified | |
association of hla-b8 has been reported with schmidt syndrome. | |||||||
6588752 | HLA (HLA) | schmidt syndrome | NA | insulin | NA | unclassified | |
we obtained peripheral blood for hla and genetic analysis from 21 relatives in a family with 8 schmidt syndrome individuals in three generations. | |||||||
6592791 | HLA (HLA) | hypoaldosteronism | NA | NA | NA | unclassified | |
linkage and segregation analysis of hla and congenital hypoaldosteronism due to corticosterone methyl-oxydase deficiency type i and type ii. |
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