CTF1

cardiotrophin 1
OMIM: 600435, Gene2Phenotype

3 panels

Panel Reviews Mode of inheritance Details
3 panels

Red CTF1 in Cardiomyopathy_Paediatric


Level 2: Cardiovascular disorders
Version 0.207

0 reviews MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown
Sources
  • South West GLH
  • Expert Review Red
  • NHS GMS

Red CTF1 in Additional findings_Paediatric


Level 2: Screening
Version 0.278

0 reviews Unknown
Sources
  • Expert Review Red
  • BabySeq Category C gene
Phenotypes
  • Cardiomyopathy, dilated

Red CTF1 in Genomic newborn screening: BabyScreen+


Level 2: Screening
Version 1.140

0 reviews Unknown
Sources
  • BabySeq Category C gene
  • Expert Review Red
Phenotypes
  • Cardiomyopathy, dilated