polycythemia, primary familial and congenital

Preferred Label : polycythemia, primary familial and congenital;

MeSH synonym : erythrocytosis, familial, 1; erythrocytosis familial, 1; familial erythrocytosis, 1; erythrocytosis autosomal dominant benign; erythrocytosis, autosomal dominant benign; primary familial polycythemia; familial erythrocytosis; benign familial polycythemia; congenital erythrocytosis; familial polycythemia; hereditary erythrocytosis; ECYT1 familial erythrocytosis-1;

Details

Origin ID

C536842;

UMLS CUI

C4551637;

Automatic exact mappings (from CISMeF team)
- Erythrocytosis, familial [OMIM phenotypic series]
CISMeF manual mappings
- Primary familial polycythemia [ORDO Disease]
Currated CISMeF NLP mapping
- Erythrocytosis, familial, 1 [OMIM Phenotype]
- Familial Polycythemia [NCIt concept]
- Familial erythrocytosis [ICD-10 Sub-category]
- Familial erythrocytosis [ICD-10 Sub-category (who)]
- Familial polycythaemia [MedDRA Preferred Term]
- Familial polycythemia [MedDRA LLT]
- Familial polycythemia [ICD-9 code]
- familial erythrocytosis 1 [DO Concept]
- hereditary pure erythrocytosis [SNOMED Notion]
- primary polycythemia [DO Concept]
MeSH term(s) associated for indexing
- polycythemia [MeSH Descriptor]
Record concept(s)
- Polycythemia, primary familial and congenital [MeSH concept]
Semantic type(s)
- Disease or Syndrome [UMLS semantic type]
UMLS correspondences (same concept)
- Erythrocytosis, familial, 1 [OMIM Phenotype]

Keyword's position in hierarchy(ies) :

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