NEURL1

neuralized E3 ubiquitin protein ligase 1
OMIM: 603804, ClinGen, DECIPHER

2 panels

Panel Reviews Mode of inheritance Details
2 panels

Red NEURL1 in Mendeliome


Version 2.61

1 review BIALLELIC, autosomal or pseudoautosomal
Sources
  • Expert Review Red
  • Literature
Phenotypes
  • Congenital hypothyroidism, MONDO:0018612, NEURL1-related

Red NEURL1 in Congenital hypothyroidism

Level 3: Thyroid disorders
Level 2: Endocrine disorders
Version 1.4

1 review BIALLELIC, autosomal or pseudoautosomal
Sources
  • Expert Review Red
  • Literature
  • Literature
Phenotypes
  • Congenital hypothyroidism, MONDO:0018612, NEURL1-related