Omodysplasia type 1 [Supplementary Concept]

mutation in GPC6

Date introduced: August 25, 2010

MeSH Unique ID: C537746

Heading Mapped to:

• Growth Disorders
• Osteochondrodysplasias/congenital

Entry Terms:

• Omodysplasia generalized form
• Omodysplasia autosomal recessive form
• Omodysplasia (Maroteaux)
• Omodysplasia 1
• Omodysplasia, Autosomal Recessive
• Omodysplasia, Generalized Form