Robinow Syndrome [Supplementary Concept]

Date introduced: November 5, 2012

MeSH Unique ID: C562492

Heading Mapped to:

• Dwarfism
• Urogenital Abnormalities
• Limb Deformities, Congenital
• Craniofacial Abnormalities

Entry Terms:

• Acral Dysostosis with Facial and Genital Abnormalities
• Fetal Face Syndrome
• Robinow Dwarfism
• Mesomelic Dwarfism-Small Genitalia Syndrome
• Robinow-Silverman-Smith Syndrome
• Robinow Syndrome, Autosomal Dominant