PanelApp (staging)
  1. Genes and Genomic Entities
  2. ARSI

ARSI

arylsulfatase family member I
OMIM: 610009, ClinGen, DECIPHER

1 panel

Panel Reviews Mode of inheritance Details
1 panel

Red ARSI in Hereditary Spastic Paraplegia - paediatric


Level 2: Neurology and neurodevelopmental disorders
Version 1.86

Component of the following Super Panels:

  • Hereditary Spastic Paraplegia Superpanel
  • Neuromuscular Superpanel
  • Progressive Neurological Conditions

    		•  1 review BIALLELIC, autosomal or pseudoautosomal
    Sources
    • Expert Review Red
    • Royal Melbourne Hospital
    Phenotypes
    • Childhood onset spastic paraplegia