MeSH Browser

MeSH Supplementary: Goldstein Hutt syndrome
Unique ID: C537282
RDF Unique Identifier: http://id.nlm.nih.gov/mesh/C537282
Entry Term(s): Long eyelashes, cataract, and hereditary spherocytosis; Trichomegaly, cataract, and hereditary spherocytosis
Registry Number: 0
Heading Mapped to: *Cataract; Eyelashes / *abnormalities; *Spherocytosis, Hereditary
Frequency: 0
Date of Entry: 2010/08/25
Revision Date: 2013/11/06

Goldstein Hutt syndrome MeSH Supplementary Concept Data 2023