Complement component c1s deficiency

Preferred Label : Complement component c1s deficiency;

Symbol : C1SD;

CISMeF acronym : C1SD;

Type : Phenotype, molecular basis known;

Alternative titles and symbols : C1s deficiency;

Prefixed ID : #613783;

Details

Origin ID

613783;

UMLS CUI

C3151078;

Automatic exact mappings (from CISMeF team)
- Immunodeficiency due to a classical component pathway complement deficiency [ORDO Disease]
Currated CISMeF NLP mapping
- complement component C1s deficiency [MeSH concept]
- complement component C1s deficiency [MeSH Supplementary Concept]
Genes related to phenotype
- Complement component 1, s subcomponent [OMIM gene]
HPO term(s)
- Abnormality of complement system [HPO term]
- Hashimoto thyroiditis [HPO term]
- Hepatitis [HPO term]
- Systemic lupus erythematosus [HPO term]
ORDO concept(s)
- Immunodeficiency due to a classical component pathway complement deficiency [ORDO Disease]
Semantic type(s)
- Disease or Syndrome [UMLS semantic type]
UMLS correspondences (same concept)
- complement component C1s deficiency [MeSH Supplementary Concept]
- complement component C1s deficiency [MeSH concept]

Keyword's position in hierarchy(ies) :

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