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Entry Name Description Category Pathway Gene
H01186 Abnormal thyroid hormone metabolism ... disorder associated with an inherited selenocysteine (Sec) incorporation defect, caused by mutations in SECISBP2 (also called SBP2). Because SBP2 is epistatic to selenoprotein synthesis, these defects have ... Endocrine and metabolic disease (THMA1) SECISBP2 [HSA:79048] [KO:K19539]
(THMA2) DIO1 [HSA:1733] [KO:K01562]
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