plasminogen deficiency, type I

Preferred Label : plasminogen deficiency, type I;

MeSH note : PROM mutation in plasminogen;

CISMeF synonym : ligneous conjunctivitis;

MeSH synonym : dysplasminogenemia;

Détails

Origin ID

C566897;

UMLS CUI

C1968804;

Automatic exact mappings (from CISMeF team)
- Hypoplasminogenemia [PASCAL descriptor]
- Ligneous conjunctivitis [ORDO Disease]
- Ligneous conjunctivitis [ICD-11 Subcategory]
- plasminogen deficiency type I [DO Concept]
DO Cross reference
- plasminogen deficiency type I [DO Concept]
MeSH term(s) associated for indexing
- conjunctivitis [MeSH Descriptor]
- plasminogen [MeSH Descriptor]
- skin diseases, genetic [MeSH Descriptor]
Record concept(s)
- ligneous conjunctivitis [MeSH concept]
- plasminogen deficiency, type I [MeSH concept]
See also inter- (CISMeF)
- Pseudomembranous conjunctivitis [PASCAL descriptor]
Semantic type(s)
- Disease or Syndrome [UMLS semantic type]
UMLS correspondences (same concept)
- Dysplasminogenemia (disorder) [SNOMED CT concept]
- Plasminogen deficiency, type I [OMIM Phenotype]
- dysplasminogenemia [SNOMED Notion]
Validated automatic mappings to NTBT
- Dysplasminogenemia [PASCAL descriptor]
- Dysplasminogenemia (disorder) [SNOMED CT concept]
- Ligneous conjunctivitis [ORDO Disease]
- Ligneous conjunctivitis [MedDRA Preferred Term]
- Ligneous conjunctivitis (disorder) [SNOMED CT concept]
- Plasminogen deficiency, type I [OMIM Phenotype]
- dysplasminogenemia [SNOMED Notion]
- ligneous conjunctivitis [Disease (Nov.)]

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