PanelApp
  1. Genes and Genomic Entities
  2. ARSI

ARSI

arylsulfatase family member I
OMIM: 610009, ClinGen, DECIPHER

2 panels

Panel Reviews Mode of inheritance Details
2 panels

Red ARSI in Mendeliome


Version 1.3795

1 review BIALLELIC, autosomal or pseudoautosomal
Sources
  • Expert Review Red
  • Expert Review
Phenotypes
  • Complex spastic paraplegia, MONDO:0015150

Red ARSI in Hereditary Spastic Paraplegia


Level 2: Neurology and neurodevelopmental disorders
Version 1.129

Component of the following Super Panels:

  • Neuromuscular Superpanel
  • Progressive Neurological Conditions

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