MeSH Browser

MeSH Supplementary: Cartilage hair hypoplasia like syndrome
Unique ID: C535915
RDF Unique Identifier: http://id.nlm.nih.gov/mesh/C535915
Registry Numbers: 0
Previous Indexing: IMMUNOLOGIC DEFICIENCY SYNDROMES (2014-2019)
Heading Mapped to: Hair / abnormalities; *Hirschsprung Disease; Osteochondrodysplasias / congenital; *Primary Immunodeficiency Diseases
Frequency: 2
Date of Entry: 2010/08/25
Revision Date: 2019/06/17

Cartilage hair hypoplasia like syndrome MeSH Supplementary Concept Data 2025