MYL9

myosin light chain 9
OMIM: 609905, Gene2Phenotype

2 panels

Panel Reviews Mode of inheritance Details
2 panels
Green MYL9 in Fetal anomalies


Level 2: Fetal (including NIPD)
Version 6.181
Latest signed off version: v6.0 (30 Apr 2025)

review BIALLELIC, autosomal or pseudoautosomal
Sources
  • NHS GMS
  • Expert Review Green
  • Expert list
Phenotypes
  • Megacystis-microcolon-intestinal hypoperistalsis syndrome 4, OMIM:619365
Green MYL9 in Paediatric pseudo-obstruction syndrome


Level 2: Gastrohepatology
Version 2.5
Latest signed off version: v2.0 (30 Apr 2025)

review BIALLELIC, autosomal or pseudoautosomal
Sources
  • Expert Review Green
  • NHS GMS
  • Expert list
Phenotypes
  • Megacystis-microcolon-intestinal hypoperistalsis syndrome 4, OMIM:619365