MeSH Browser

MeSH Supplementary: Kotzot-Richter syndrome
Unique ID: C537025
RDF Unique Identifier: http://id.nlm.nih.gov/mesh/C537025
Entry Term(s): Albinism with immune and hematologic defects; Oculocutaneous albinism, immunodeficiency, hematological disorders, and minor anomalies
Registry Number: 0
Previous Indexing: IMMUNOLOGIC DEFICIENCY SYNDROMES (2013-2019)
Heading Mapped to: *Primary Immunodeficiency Diseases; *Hermanski-Pudlak Syndrome
Frequency: 2
Date of Entry: 2010/08/25
Revision Date: 2019/06/17

Kotzot-Richter syndrome MeSH Supplementary Concept Data 2023