has material basis in germline mutation in ALB hereditary disease hyperthyroidism hyperthyroxinemia hyperthyroxinemia, familial dysalbuminemic https://github.com/monarch-initiative/mondo/issues/4521 https://www.malacards.org/card/hyperthyroxinemia_familial_dysalbuminemic familial Dysalbuminemic hyperthyroidism dysalbuminemic hypertriiodothyroninemia hyperthyroxinemia, familial dysalbuminemic MESH:D050010 bisalbuminemia UMLS:C0342185 FDAH SCTID:237547004 FDH familial Dysalbuminemic hyperthyroxinemia hyperthyroxinemia, familial Dysalbuminemic dysalbuminemic hyperthyroxinemia OMIM:615999 Orphanet:276271 NCIT:C131813 An inherited autosomal dominant trait characterized by abnormally elevated levels of total serum thyroxine; (T4) in euthyroid patients with abnormal serum albumin that binds T4 with enhanced affinity. The serum levels of free T4, free T3, and tsh are normal. It is one of several T4 abnormalities produced by non-thyroid disorder. This condition is due to mutations of the alb gene on chromosome 4. MEDGEN:90974 MONDO:0014448