TPO

thyroid peroxidase
OMIM: 606765, Gene2Phenotype

4 panels

Panel Reviews Mode of inheritance Details
4 panels

Red TPO in Autism


Version 0.27

review Not set
Sources
  • Expert Review Red
  • SFARI

Green TPO in Congenital hypothyroidism

Level 3: Thyroid disorders
Level 2: Endocrine disorders
Version 2.4
Latest signed off version: v2.2 (25 Feb 2020)

review BIALLELIC, autosomal or pseudoautosomal
Sources
  • Expert Review Green
  • Eligibility statement prior genetic testing
  • UKGTN
  • Illumina TruGenome Clinical Sequencing Services
Phenotypes
  • Congenital hypothyroidism
  • Thyroid dyshormonogenesis 2A, 274500
  • TDH2A
  • Iodide organification defect
  • goitre
Tags
  • monogenic-polygenic

Green TPO in Severe Paediatric Disorders


Version 1.66

review BIALLELIC, autosomal or pseudoautosomal
Sources
  • Next Generation Children Project
  • Expert Review Green
  • Expert list
Phenotypes
  • Thyroid dyshormonogenesis 2A, 274500

Green TPO in NewbornFullV1


Version 0.1

review BIALLELIC, autosomal or pseudoautosomal
Sources
  • Expert Review Green