TTF1

transcription termination factor 1
OMIM: 600777, Gene2Phenotype

2 panels

Panel Reviews Mode of inheritance Details
2 panels

Amber TTF1 in Mendeliome


Version 1.1891

review MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
Sources
  • Expert Review Amber
  • Victorian Clinical Genetics Services
Phenotypes
  • congenital hypothyroidism, thyroid dysgenesis, No OMIM #

Amber TTF1 in Congenital hypothyroidism

Level 3: Thyroid disorders
Level 2: Endocrine disorders
Version 0.43

review MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
Sources
  • Expert Review Amber
  • Literature
Phenotypes
  • congenital hypothyroidism, thyroid dysgenesis, No OMIM #