has material basis in germline mutation in TPO familial thyroid dyshormonogenesis thyroid dyshormonogenesis 2A https://www.malacards.org/card/thyroid_dyshormonogenesis_2a MEDGEN:226940 DOID:0112186 UMLS:C1291299 familial thyroid dyshormonogenesis caused by mutation in TPO thyroid dyshormonogenesis type 2A GARD:0018189 thyroid hormonogenesis, genetic defect in, 2A TDH2A MESH:C563206 TPO familial thyroid dyshormonogenesis MONDO:0010133 Thyroid peroxidase system defect due to presumed mutation(s) in the TPO gene, resulting in decreased activity of thyroid peroxidase. NCIT:C121750 OMIM:274500 thyroid dyshormonogenesis 2A ICD9:277.6 SCTID:124204003 hypothyroidism, congenital, due to dyshormonogenesis, 2A