TCF7L1:Ensemblv115

transcription factor 7 like 1
OMIM: 604652, ClinGen, DECIPHER

1 panel

Panel Reviews Mode of inheritance Details
1 panel

Red TCF7L1 in Pituitary hormone deficiency

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

1 review MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown
Sources
  • Genomics England PanelApp
  • Expert Review Red
Phenotypes
  • Combined pituitary deficiencies, genetic form, MONDO:0013099, TCF7L1-related