Osteopetrosis, mild autosomal recessive form [Supplementary Concept]

Optb2 not included

Date introduced: August 25, 2010

MeSH Unique ID: C536059

Heading Mapped to:

• Osteopetrosis/congenital

Entry Terms:

• Mild autosomal recessive form of osteopetrosis
• Osteopetrosis, Autosomal Recessive 2
• Osteopetrosis, Osteoclast-Poor