GAL

galanin and GMAP prepropeptide
OMIM: 137035, Gene2Phenotype

2 panels

Panel Reviews Mode of inheritance Details
2 panels
Red GAL in Familial Hirschsprung Disease

Level 3: Gastrointestinal disorders
Level 2: Gastroenterological disorders
Version 1.11

review Unknown
Sources
  • Expert Review Red
  • Literature
Phenotypes
  • Hirschsprung disease
  • HD
Red GAL in Early onset or syndromic epilepsy


Level 2: Neurology
Version 8.125
Latest signed off version: v8.0 (30 Apr 2025)

Component of the following Super Panels:

  • Paediatric disorders
  • Unexplained death in infancy and sudden unexplained death in childhood
  • review MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown
    Sources
    • Wessex and West Midlands GLH
    • NHS GMS
    • Expert Review Red
    • Literature
    Phenotypes
    • ?Epilepsy, familial temporal lobe, 8 616461