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Drug Target Ontology
Last uploaded:
February 15, 2018
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Preferred Name | complement deficiency | |
Synonyms |
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Definitions |
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. |
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ID |
http://purl.obolibrary.org/obo/DOID_626 |
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definition |
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.
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hasDbXref |
SNOMEDCT_US_2016_03_01:24743004 NCI:C4691 SNOMEDCT_US_2016_03_01:191014008 UMLS_CUI:C0272242 ICD10CM:D80-D89 ICD10CM:D84.1
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hasExactSynonym |
Complement deficiency disease (disorder) Complement deficiency
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hasOBONamespace |
disease_ontology
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id |
DOID:626
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imported from | ||
label |
complement deficiency
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prefixIRI |
DOID:626
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prefLabel |
complement deficiency
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subClassOf |
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