MeSH Browser

MeSH Supplementary: Complement component 5 deficiency
Unique ID: C537005
RDF Unique Identifier: http://id.nlm.nih.gov/mesh/C537005
Entry Term(s): Dysfunction of the fifth component of complement (C5); Leiner disease
Registry Numbers: 0
Previous Indexing: IMMUNOLOGIC DEFICIENCY SYNDROMES (2014-2019)
Heading Mapped to: Complement C5 / deficiency; *Hereditary Complement Deficiency Diseases
Frequency: 121
Note: Dysfunction of complement 5 due to homozygous or compound heterozygous mutation in the C5 gene and characterized by SEBORRHEIC DERMATITIS, intractable diarrhea, GRAM-NEGATIVE BACTERIAL INFECTIONS, and severe wasting. OMIM: 609536
Date of Entry: 2010/08/25
Revision Date: 2021/11/29

Complement component 5 deficiency MeSH Supplementary Concept Data 2025