familial thyroid dyshormonogenesis https://github.com/monarch-initiative/mondo/issues/642 https://www.malacards.org/card/familial_thyroid_dyshormonogenesis MEDGEN:903446 thyroid dyshormonogenesis MONDO:0010132 MESH:C564766 UMLS:C4273748 OMIMPS:274400 dyshormonogenesis NCIT:C121751 A type of primary congenital hypothyroidism, a permanent thyroid hormone deficiency that is present from birth, which results from inborn errors of thyroid hormone synthesis. GARD:0016843 DOID:0112183 SCTID:718183003 Orphanet:95716 nongoitrous hyperthyrotropinemia congenital hypothyroidism inherited thyroid metabolism disease