PanelApp (stage)
  1. Genes and Genomic Entities
  2. MYO1H

MYO1H

myosin IH
OMIM: 614636, Gene2Phenotype

2 panels

Panel Reviews Mode of inheritance Details
2 panels

Red MYO1H in Central Hypoventilation


Level 2: Neurology and neurodevelopmental disorders
Version 1.5

review BIALLELIC, autosomal or pseudoautosomal
Sources
  • Expert Review Red
  • Literature
Phenotypes
  • Central hypoventilation syndrome, congenital, 2, and autonomic dysfunction, MIM#619482

Red MYO1H in Mendeliome


Version 1.1891

review BIALLELIC, autosomal or pseudoautosomal
Sources
  • Expert Review Red
  • Literature
Phenotypes
  • Central hypoventilation syndrome, congenital, 2, and autonomic dysfunction, MIM#619482