PIGL

phosphatidylinositol glycan anchor biosynthesis class L
OMIM: 605947, ClinGen, DECIPHER

10 panels

Panel Reviews Mode of inheritance Details
10 panels

Green PIGL in Anophthalmia_Microphthalmia_Coloboma


Level 2: Ophthalmological disorders
Version 2.0

1 review BIALLELIC, autosomal or pseudoautosomal
Sources
  • Expert Review Green
  • Expert Review
Phenotypes
  • CHIME syndrome, MIM# 280000, MONDO:0010221
Tags
  • SV/CNV
  • founder

Green PIGL in Congenital Disorders of Glycosylation


Level 2: Metabolic disorders
Version 2.0

1 review BIALLELIC, autosomal or pseudoautosomal
Sources
  • Expert Review Green
  • Victorian Clinical Genetics Services
Phenotypes
  • CHIME syndrome, MIM# 280000, MONDO:0010221
Tags
  • SV/CNV
  • founder

Green PIGL in Congenital Heart Defect


Level 2: Cardiovascular disorders
Version 1.0

1 review BIALLELIC, autosomal or pseudoautosomal
Sources
  • Expert Review Green
  • Literature
Phenotypes
  • CHIME syndrome, MIIM# 280000

Green PIGL in Ichthyosis and Porokeratosis


Level 2: Dermatological disorders
Version 2.0

2 reviews BIALLELIC, autosomal or pseudoautosomal
Sources
  • Expert Review Green
  • Literature
Phenotypes
  • CHIME syndrome, MIM# 280000, MONDO:0010221
Tags
  • SV/CNV
  • founder

Green PIGL in Mendeliome


Version 2.0

1 review BIALLELIC, autosomal or pseudoautosomal
Sources
  • Expert Review Green
  • Victorian Clinical Genetics Services
Phenotypes
  • CHIME syndrome, MIM# 280000, MONDO:0010221
Tags
  • SV/CNV
  • founder

Green PIGL in Intellectual disability syndromic and non-syndromic


Level 2: Neurology and neurodevelopmental disorders
Version 2.0

1 review BIALLELIC, autosomal or pseudoautosomal
Sources
  • Expert Review Green
  • Genetic Health Queensland
Phenotypes
  • CHIME syndrome, MIM# 280000, MONDO:0010221
Tags
  • SV/CNV
  • founder

Green PIGL in Mackenzie's Mission_Reproductive Carrier Screening


Level 2: Screening
Version 1.0

0 reviews BIALLELIC, autosomal or pseudoautosomal
Sources
  • Expert Review Green
  • Mackenzie's Mission
Phenotypes
  • CHIME syndrome, 280000 (3)

Red PIGL in Clefting disorders

Level 3: Dysmorphic disorders
Level 2: Dysmorphic and congenital abnormality syndromes
Version 1.0

0 reviews BIALLELIC, autosomal or pseudoautosomal
Sources
  • Expert Review Red
Phenotypes
  • CHIME
  • COLOBOMA, CONGENITAL HEART DISEASE, ICHTHYOSIFORM DERMATOSIS, MENTAL RETARDATION, AND EAR ANOMALIES SYNDROME

Green PIGL in Fetal anomalies


Version 2.0

2 reviews BIALLELIC, autosomal or pseudoautosomal
Sources
  • Expert Review Green
  • Genomics England PanelApp
  • Genetic Health Queensland
Phenotypes
  • CHIME syndrome, MIM# 280000, MONDO:0010221
Tags
  • SV/CNV

Green PIGL in Prepair 1000+


Level 2: Screening
Version 3.0

1 review BIALLELIC, autosomal or pseudoautosomal
Sources
  • Expert Review Green
  • Mackenzie's Mission
Phenotypes
  • CHIME syndrome, MIM# 280000, MONDO:0010221