BMPR1A Gene Mutation

**Semantic type:** Cell or Molecular Dysfunction

**Definition:** A molecular genetic abnormality that refers to the mutation of the BMPR1A (bone morphogenetic protein receptor, type 1A) gene on chromosome 10q22.3.

**Synonyms:** - ACVRLK3 Gene Mutation - ALK3 Gene Mutation - Bone Morphogenetic Protein Receptor Type 1A Gene Mutation - SKR5 Gene Mutation