TMPRSS9

transmembrane protease, serine 9
OMIM: 610477, Gene2Phenotype

2 panels

Panel Reviews Mode of inheritance Details
2 panels
Red TMPRSS9 in Autism


Version 0.36

review BIALLELIC, autosomal or pseudoautosomal
Sources
  • Expert Review Red
  • Literature
Phenotypes
  • Progressive intellectual and neurological deterioration
  • Global developmental delay
  • Intellectual disability
  • Autism
  • Epilepsy
Red TMPRSS9 in Intellectual disability

Level 3: Neurodevelopmental disorders
Level 2: Neurology and neurodevelopmental disorders
Version 6.11
Latest signed off version: v6.0 (1 May 2024)

Component of the following Super Panels:

  • Childhood onset leukodystrophy
  • Hypotonic infant
  • Paediatric disorders
  • review BIALLELIC, autosomal or pseudoautosomal
    Sources
    • Other
    Phenotypes
    • Progressive intellectual and neurological deterioration
    • Global developmental delay
    • Intellectual disability
    • Autism
    • Epilepsy
    Tags
    • watchlist