Complement component 9 deficiency

Preferred Label : Complement component 9 deficiency;

Symbol : C9D;

CISMeF acronym : C9D;

Type : Phenotype, molecular basis known;

Alternative titles and symbols : C9 deficiency;

Prefixed ID : #613825;

Details

Origin ID

613825;

UMLS CUI

C3151189;

Automatic exact mappings (from CISMeF team)
- C9 deficiency [MeSH concept]
- Immunodeficiency due to a late component of complement deficiency [ORDO Disease]
CISMeF manual mappings
- Complement component C9 deficiency [ICD-11 More detail]
Currated CISMeF NLP mapping
- C9 deficiency [MeSH Supplementary Concept]
- complement component 9 deficiency [DO Concept]
DO Cross reference
- complement component 9 deficiency [DO Concept]
Genes related to phenotype
- Complement component 9 [OMIM gene]
HPO term(s)
- Decreased serum complement C9 [HPO term]
ORDO concept(s)
- Immunodeficiency due to a late component of complement deficiency [ORDO Disease]
Semantic type(s)
- Disease or Syndrome [UMLS semantic type]
UMLS correspondences (same concept)
- C9 deficiency [MeSH Supplementary Concept]
- C9 deficiency [MeSH concept]
- Complement component C9 deficiency [ICD-11 More detail]
- complement component 9 deficiency [DO Concept]

Keyword's position in hierarchy(ies) :

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