MeSH Browser

MeSH Supplementary: Neutropenia, Severe Congenital, Autosomal Recessive 4
Unique ID: C567260
RDF Unique Identifier: http://id.nlm.nih.gov/mesh/C567260
Entry Term(s): Dursun Syndrome; Pulmonary Arterial Hypertension, Leukopenia, And Atrial Septal Defect; Scn4
Registry Numbers: 0
Heading Mapped to: *Neutropenia
Frequency: 5
Note: aka SCN4
Date of Entry: 2012/11/05
Revision Date: 2021/11/15

Neutropenia, Severe Congenital, Autosomal Recessive 4 MeSH Supplementary Concept Data 2025