Hypertrichosis Terminalis, Generalized, with or without Gingival Hyperplasia [Supplementary Concept]

Date introduced: November 5, 2012

MeSH Unique ID: C565016

Heading Mapped to:

• Chromosome Deletion
• Chromosomes, Human, Pair 17
• Fibromatosis, Gingival
• Hypertrichosis

Entry Terms:

• Fibromatosis, Gingival, with Hypertrichosis
• Microdeletion 17q24.2-q24.3 Syndrome
• Chromosome 17q24.2-q24.3 Deletion Syndrome