STAB2

stabilin 2
OMIM: 608561, ClinGen, DECIPHER

1 panel

Panel Reviews Mode of inheritance Details
1 panel

Red STAB2 in Bleeding and Platelet Disorders


Level 2: Haematological disorders
Version 2.0

1 review MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown
Sources
  • Literature
  • Expert Review Red
Phenotypes
  • Chronic thromboembolic pulmonary hypertension MONDO:0013024, STAB2-related