Potocki-Shaffer syndrome [Supplementary Concept]

MeSH Unique ID: C538356

Heading Mapped to:

• Chromosome Deletion
• Chromosomes, Human, Pair 11
• Exostoses, Multiple Hereditary
• Chromosome Disorders

Entry Terms:

• Defect11 Syndrome
• P11PDS
• Proximal 11P deletion syndrome
• Chromosome 11p11.2 Deletion Syndrome
• Exostoses, Multiple, Type II
• Deletion of chromosome 11p11.2