GLA

Panel	Reviews	Mode of inheritance	Details
Filter panels 25 panels
Green GLA in Early-onset Dementia Level 2: Neurology and neurodevelopmental disorders Version 1.24 Component of the following Super Panels: Neurodegenerative disease - adult onset Progressive Neurological Conditions	review	X-LINKED: hemizygous mutation in males, monoallelic mutations in females may cause disease (may be less severe, later onset than males)	Sources Expert Review Green Literature Phenotypes Fabry disease MONDO:0010526
Green GLA in Vasculitis Level 2: Immunological disorders Version 0.82	review	Unknown	Sources Victorian Clinical Genetics Services Expert Review Green
Amber GLA in Brain Calcification Level 2: Neurology and neurodevelopmental disorders Version 1.96 Component of the following Super Panels: Progressive Neurological Conditions	review	X-LINKED: hemizygous mutation in males, biallelic mutations in females	Sources Expert Review Amber Expert list Phenotypes Fabry disease, MIM# 301500
Green GLA in Hypertrophic cardiomyopathy_HCM Level 2: Cardiovascular disorders Version 0.178 Component of the following Super Panels: Adult Cardiac SuperPanel Cardiomyopathy_Adult_SuperPanel	review	X-LINKED: hemizygous mutation in males, monoallelic mutations in females may cause disease (may be less severe, later onset than males)	Sources Expert Review Green Victorian Clinical Genetics Services Phenotypes Fabry disease (MIM# 301500)
Red GLA in Hydrops fetalis Level 2: Dysmorphic and congenital abnormality syndromes Version 0.313	review	X-LINKED: hemizygous mutation in males, biallelic mutations in females	Sources Expert Review Red Victorian Clinical Genetics Services Phenotypes Fabry disease, MIM# 301500
Green GLA in Incidentalome Version 0.301	review	X-LINKED: hemizygous mutation in males, monoallelic mutations in females may cause disease (may be less severe, later onset than males)	Sources Expert Review Green Expert Review Green Victorian Clinical Genetics Services Victorian Clinical Genetics Services Phenotypes Fabry disease 301500 Fabry disease, cardiac variant 301500 Tags cardiac
Green GLA in Proteinuria Level 2: Renal and urinary tract disorders Version 0.225 Component of the following Super Panels: Kidneyome_SuperPanel Renal Glomerular Disease_SuperPanel	review	X-LINKED: hemizygous mutation in males, biallelic mutations in females	Sources Expert Review Green Expert list Phenotypes Fabry disease, MIM# 301500
Green GLA in Lysosomal Storage Disorder Level 2: Metabolic conditions Version 1.11 Component of the following Super Panels: Metabolic Disorders Superpanel Progressive Neurological Conditions	review	X-LINKED: hemizygous mutation in males, biallelic mutations in females	Sources Expert Review Green Victorian Clinical Genetics Services Phenotypes Fabry disease, MIM# 301500 MONDO:0010526
Green GLA in Regression Level 2: Neurology and neurodevelopmental disorders Version 0.556	review	Unknown	Sources Victorian Clinical Genetics Services Expert Review Green
Green GLA in Additional findings_Adult Level 2: Screening Version 0.166	review	X-LINKED: hemizygous mutation in males, monoallelic mutations in females may cause disease (may be less severe, later onset than males)	Sources Expert Review Green Melbourne Genomics Health Alliance Phenotypes Fabry disease, MIM# 301500
Green GLA in Leukodystrophy - adult onset Level 2: Neurology and neurodevelopmental disorders Version 0.140 Component of the following Super Panels: Leukodystrophy_Superpanel Progressive Neurological Conditions	review	X-LINKED: hemizygous mutation in males, biallelic mutations in females	Sources Royal Melbourne Hospital Expert Review Green Phenotypes Fabry disease, Fabry disease, cardiac variant, 301500
Green GLA in Hereditary Neuropathy - complex Level 2: Neurology and neurodevelopmental disorders Version 1.14 Component of the following Super Panels: Hereditary Neuropathy_CMT_IsolatedAndComplex Neuromuscular Superpanel Progressive Neurological Conditions	review	X-LINKED: hemizygous mutation in males, monoallelic mutations in females may cause disease (may be less severe, later onset than males)	Sources Expert Review Green Royal Melbourne Hospital Phenotypes Cardiomyopathy HSAN/SFN Fabry disease
Green GLA in Pain syndromes Level 2: Neurology and neurodevelopmental disorders Version 0.34 Component of the following Super Panels: Progressive Neurological Conditions	review	X-LINKED: hemizygous mutation in males, monoallelic mutations in females may cause disease (may be less severe, later onset than males)	Sources Expert Review Green Genomics England PanelApp Phenotypes Fabry disease, 301500
Green GLA in Mackenzie's Mission_Reproductive Carrier Screening Level 2: Screening Version 0.109	review	X-LINKED: hemizygous mutation in males, biallelic mutations in females	Sources Expert Review Green Mackenzie's Mission Phenotypes Fabry disease, 301500 (3)
Green GLA in Stroke Level 2: Neurology and neurodevelopmental disorders Version 1.16	review	X-LINKED: hemizygous mutation in males, biallelic mutations in females	Sources Expert Review Green Royal Melbourne Hospital Phenotypes Fabry disease, MIM# 301500, MONDO:0010526
Red GLA in Cerebral vascular malformations Level 2: Neurology and neurodevelopmental disorders Version 0.39 Component of the following Super Panels: Progressive Neurological Conditions	review	Unknown	Sources Genomics England PanelApp Expert Review Red Phenotypes Moyamoya disease
Amber GLA in Cardiomyopathy_Paediatric Level 2: Cardiovascular disorders Version 0.192	review	X-LINKED: hemizygous mutation in males, monoallelic mutations in females may cause disease (may be less severe, later onset than males)	Sources South West GLH NHS GMS Expert Review Amber MetBioNet London South GLH Phenotypes Fabry disease, cardiac variant, 301500 Fabry disease (Sphingolipidoses) Fabry disease, 301500 Fabry Disease HCM syndromic HCM Limb pain, angiokeratom Fabry disease HCM is a late complication in adults, also found in female carriers
Green GLA in Additional findings_Paediatric Level 2: Screening Version 0.278	review	X-LINKED: hemizygous mutation in males, biallelic mutations in females	Sources BabySeq Category A gene Expert Review Green Phenotypes Fabry disease
Green GLA in Incidentalome_PREGEN_DRAFT Version 0.43	review	Unknown	Sources NSW Health Pathology Expert Review Green
Red GLA in Fetal anomalies Version 1.255	review	X-LINKED: hemizygous mutation in males, monoallelic mutations in females may cause disease (may be less severe, later onset than males)	Sources Expert Review Red Genomics England PanelApp Phenotypes Fabry disease, 301500
Green GLA in Prepair 1000+ Level 2: Screening Version 1.9	review	X-LINKED: hemizygous mutation in males, biallelic mutations in females	Sources Expert Review Green Mackenzie's Mission Phenotypes Fabry disease, MIM#301500
Green GLA in BabyScreen+ newborn screening Level 2: Screening Version 1.114	review	X-LINKED: hemizygous mutation in males, biallelic mutations in females	Sources Expert Review Green BabySeq Category A gene Phenotypes Fabry disease (MIM# 301500) Tags treatable metabolic
Green GLA in Renal Tubulopathies and related disorders Level 2: Renal and urinary tract disorders Version 1.14 Component of the following Super Panels: Kidneyome_SuperPanel	review	X-LINKED: hemizygous mutation in males, monoallelic mutations in females may cause disease (may be less severe, later onset than males)	Sources Expert Review Green KidGen_MetabolicRenal v38.1.0 Phenotypes Fabry disease (MIM# 301500)
Green GLA in Transplant Co-Morbidity Superpanel Level 2: Screening Version 0.18	review	X-LINKED: hemizygous mutation in males, monoallelic mutations in females may cause disease (may be less severe, later onset than males)	Sources Expert Review Green Victorian Clinical Genetics Services Phenotypes Fabry disease (MIM# 301500)
Green GLA in Prepair 500+ Level 2: Screening Version 1.1	review	X-LINKED: hemizygous mutation in males, biallelic mutations in females	Sources Expert Review Green Mackenzie's Mission Phenotypes Fabry disease, MIM#301500

GLA

25 panels

Green GLA in Early-onset Dementia

Sources

Phenotypes

Green GLA in Vasculitis

Sources

Amber GLA in Brain Calcification

Sources

Phenotypes

Green GLA in Hypertrophic cardiomyopathy_HCM

Sources

Phenotypes

Red GLA in Hydrops fetalis

Sources

Phenotypes

Green GLA in Incidentalome

Sources

Phenotypes

Tags

Green GLA in Proteinuria

Sources

Phenotypes

Green GLA in Lysosomal Storage Disorder

Sources

Phenotypes

Green GLA in Regression

Sources

Green GLA in Additional findings_Adult

Sources

Phenotypes

Green GLA in Leukodystrophy - adult onset

Sources

Phenotypes

Green GLA in Hereditary Neuropathy - complex

Sources

Phenotypes

Green GLA in Pain syndromes

Sources

Phenotypes

Green GLA in Mackenzie's Mission_Reproductive Carrier Screening

Sources

Phenotypes

Green GLA in Stroke

Sources

Phenotypes

Red GLA in Cerebral vascular malformations

Sources

Phenotypes

Amber GLA in Cardiomyopathy_Paediatric

Sources

Phenotypes

Green GLA in Additional findings_Paediatric

Sources

Phenotypes

Green GLA in Incidentalome_PREGEN_DRAFT

Sources

Red GLA in Fetal anomalies

Sources

Phenotypes

Green GLA in Prepair 1000+

Sources

Phenotypes

Green GLA in BabyScreen+ newborn screening

Sources

Phenotypes

Tags

Green GLA in Renal Tubulopathies and related disorders

Sources

Phenotypes

Green GLA in Transplant Co-Morbidity Superpanel

Sources

Phenotypes

Green GLA in Prepair 500+

Sources

Phenotypes