PDIA6

protein disulfide isomerase family A member 6
OMIM: 611099, ClinGen, DECIPHER

7 panels

Panel Reviews Mode of inheritance Details
7 panels

Green PDIA6 in Ciliopathies


Level 2: Dysmorphic and congenital abnormality syndromes
Version 2.0

3 reviews BIALLELIC, autosomal or pseudoautosomal
Sources
  • Expert Review Green
  • Expert Review
Phenotypes
  • multiple congenital anomalies, MONDO:0019042, PDIA6-related

Green PDIA6 in Mendeliome


Version 2.0

3 reviews BIALLELIC, autosomal or pseudoautosomal
Sources
  • Expert Review Green
  • Literature
  • Literature
Phenotypes
  • multiple congenital anomalies, MONDO:0019042, PDIA6-related

Green PDIA6 in Skeletal Ciliopathies


Level 2: Skeletal disorders
Version 2.0

3 reviews BIALLELIC, autosomal or pseudoautosomal
Sources
  • Expert Review Green
  • Literature
Phenotypes
  • multiple congenital anomalies, MONDO:0019042, PDIA6-related

Green PDIA6 in Renal Ciliopathies and Nephronophthisis


Level 2: Renal and urinary tract disorders
Version 2.0

3 reviews BIALLELIC, autosomal or pseudoautosomal
Sources
  • Expert Review Green
  • Literature
Phenotypes
  • multiple congenital anomalies, MONDO:0019042, PDIA6-related

Green PDIA6 in Skeletal dysplasia

Level 3: Skeletal dysplasias
Level 2: Skeletal disorders
Version 1.0

3 reviews BIALLELIC, autosomal or pseudoautosomal
Sources
  • Expert Review Green
  • Literature
  • Literature
  • Literature
  • Literature
Phenotypes
  • multiple congenital anomalies, MONDO:0019042, PDIA6-related

Green PDIA6 in Monogenic Diabetes


Level 2: Endocrine disorders
Version 1.0

3 reviews BIALLELIC, autosomal or pseudoautosomal
Sources
  • Expert Review Green
  • Literature
Phenotypes
  • multiple congenital anomalies, MONDO:0019042, PDIA6-related

Green PDIA6 in Fetal anomalies


Version 2.0

3 reviews BIALLELIC, autosomal or pseudoautosomal
Sources
  • Expert Review Green
  • Literature
Phenotypes
  • multiple congenital anomalies, MONDO:0019042, PDIA6-related