MeSH Browser

MeSH Supplementary: FLOTCH syndrome
Unique ID: C537065
RDF Unique Identifier: http://id.nlm.nih.gov/mesh/C537065
Entry Term(s): Friedel Heid Grosshans syndrome
Registry Numbers: 0
Heading Mapped to: *Blepharitis; *Epidermal Cyst; *Hair Diseases; Nail Diseases / congenital; *Pigmentation Disorders; *Retinal Diseases
Frequency: 1
Note: Familial occurrence of total Leukonychia, Trichilemmal cysts and Ciliary dystrophy with dominant autosomal Heredity
Source: Ann Dermatol Venereol. 1986;113(6-7):549-53
Date of Entry: 2010/08/25
Revision Date: 2013/11/06

FLOTCH syndrome MeSH Supplementary Concept Data 2025