TPO

thyroid peroxidase
OMIM: 606765, Gene2Phenotype

2 panels

Panel Reviews Mode of inheritance Details
2 panels
Red TPO in Fetal anomalies


Level 2: Fetal (including NIPD)
Version 6.140
Latest signed off version: v6.0 (30 Apr 2025)

review BIALLELIC, autosomal or pseudoautosomal
Sources
  • Expert Review Red
  • NHS GMS
Phenotypes
  • Thyroid dyshormonogenesis 2A, OMIM:274500
Green TPO in Congenital hypothyroidism


Level 2: Endocrinology
Version 3.3
Latest signed off version: v3.0 (30 Apr 2025)

review BIALLELIC, autosomal or pseudoautosomal
Sources
  • Expert Review Green
  • Eligibility statement prior genetic testing
  • UKGTN
  • Illumina TruGenome Clinical Sequencing Services
Phenotypes
  • Thyroid dyshormonogenesis 2A, OMIM:274500
Tags
  • monogenic-polygenic