KRT18

keratin 18
OMIM: 148070, ClinGen, DECIPHER

3 panels

Panel Reviews Mode of inheritance Details
3 panels

Red KRT18 in Mendeliome


Version 1.2302

1 review Unknown
Sources
  • Expert Review Red
  • Victorian Clinical Genetics Services
Phenotypes
  • Cirrhosis, cryptogenic , MIM#215600

Red KRT18 in Additional findings_Paediatric


Level 2: Screening
Version 0.278

0 reviews MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
Sources
  • Expert Review Red
  • BabySeq Category C gene
Phenotypes
  • Cirrhosis, cryptogenic

Red KRT18 in BabyScreen+ newborn screening


Level 2: Screening
Version 1.116

0 reviews MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
Sources
  • BabySeq Category C gene
  • Expert Review Red
Phenotypes
  • Cirrhosis, cryptogenic