MeSH Browser

MeSH Supplementary: Hypertrichosis Terminalis, Generalized, with or without Gingival Hyperplasia
Unique ID: C565016
RDF Unique Identifier: http://id.nlm.nih.gov/mesh/C565016
Entry Term(s): Chromosome 17q24.2-q24.3 Deletion Syndrome; Fibromatosis, Gingival, with Hypertrichosis; Microdeletion 17q24.2-q24.3 Syndrome
Registry Numbers: 0
Heading Mapped to: *Chromosome Deletion; Chromosomes, Human, Pair 17; *Fibromatosis, Gingival; *Hypertrichosis
Frequency: 4
Date of Entry: 2012/11/05
Revision Date: 1955/01/01

Hypertrichosis Terminalis, Generalized, with or without Gingival Hyperplasia MeSH Supplementary Concept Data 2025