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DO Term : complement deficiency [DOID:626] Disease Ontology

Namespace  disease_ontology Obsolete  false
description  A primary immunodeficiency disease that is the result in a mutation of a gene encoding one of the thirty complement system proteins, produced predominantly in liver, which function to defend against infection and produce inflammation.
  • synonyms:
  • MESH:D000081208,
  • ICD10CM:D84.1,
  • SNOMEDCT_US_2023_03_01:191014008,
  • Complement deficiency disease,
  • UMLS_CUI:C0272242,
  • NCI:C4691
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Disease

Diseases --> Human genes

Diseases --> Mouse genes

Diseases --> Mouse models

Ontology

Ontology Term --> All ancestors

Ontology Term --> All descendants

Ontology Term --> Direct children

Ontology Term --> Direct parents