1. Genes and Genomic Entities
  2. INMT

INMT

indolethylamine N-methyltransferase
OMIM: 604854, Gene2Phenotype

1 panel

Panel Reviews Mode of inheritance Details
1 panel
Red INMT in Familial Hirschsprung Disease

Level 3: Gastrointestinal disorders
Level 2: Gastroenterological disorders
Version 1.10

review Unknown
Sources
  • Expert Review Red
  • Literature
Phenotypes
  • risk of HSCR