MeSH Browser

MeSH Supplementary: Macules hereditary congenital hypopigmented and hyperpigmented
Unique ID: C537836
RDF Unique Identifier: http://id.nlm.nih.gov/mesh/C537836
Entry Term(s): Congenital hypomelanotic and hypermelanotic macules; Hereditary congenital hypopigmented and hyperpigmented macules; Macules, Hereditary Congenital Hypopigmented and Hyperpigmented; Westerhof Beemer Cormane syndrome
Heading Mapped to: *Pigmentation Disorders
Frequency: 4
Date of Entry: 2010/08/25
Revision Date: 2012/11/05

Macules hereditary congenital hypopigmented and hyperpigmented MeSH Supplementary Concept Data 2024