ARSI

arylsulfatase family member I
OMIM: 610009, Gene2Phenotype

1 panel

Panel	Reviews	Mode of inheritance	Details
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	review	BIALLELIC, autosomal or pseudoautosomal	Sources Expert Review Red Royal Melbourne Hospital Phenotypes Childhood onset spastic paraplegia

Panel

Reviews

Mode of inheritance

Details

Level 2: Neurology and neurodevelopmental disorders
Version 1.86

Component of the following Super Panels:

Hereditary Spastic Paraplegia Superpanel

Neuromuscular Superpanel

Progressive Neurological Conditions

review

BIALLELIC, autosomal or pseudoautosomal