PTPN13

protein tyrosine phosphatase, non-receptor type 13
OMIM: 600267, Gene2Phenotype

3 panels

Panel Reviews Mode of inheritance Details
3 panels

Amber PTPN13 in Bone Marrow Failure


Level 2: Haematological disorders
Version 1.93

review BIALLELIC, autosomal or pseudoautosomal
Sources
  • Expert Review Amber
  • Literature
Phenotypes
  • bone marrow failure syndrome MONDO#0000159, PTPN13-related

Amber PTPN13 in Mendeliome


Version 1.1902

review BIALLELIC, autosomal or pseudoautosomal
Sources
  • Expert Review Amber
  • Literature
Phenotypes
  • bone marrow failure syndrome MONDO#0000159, PTPN13-related

Red PTPN13 in CGC_86


Version 0.2

review Other
Sources
  • CGC_86
Phenotypes
  • NA