TTF2

transcription termination factor 2
OMIM: 604718, Gene2Phenotype

2 panels

Panel Reviews Mode of inheritance Details
2 panels

Red TTF2 in Mendeliome


Version 1.1891

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

Red TTF2 in Congenital hypothyroidism

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

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