TTF2:Ensemblv115

transcription termination factor 2
OMIM: 604718, ClinGen, DECIPHER

1 panel

Panel Reviews Mode of inheritance Details
1 panel

Red TTF2 in Congenital hypothyroidism

Level 3: Thyroid disorders
Level 2: Endocrine disorders
Version 1.0

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