pyropoikilocytosis, hereditary

Preferred Label : pyropoikilocytosis, hereditary;

Origin ID

C563004;

UMLS CUI

C0520739;

Currated CISMeF NLP mapping
- Hereditary Pyropoikilocytosis [NCIt concept]
- Hereditary pyropoikilocytosis [ICD-11 More detail]
- Hereditary pyropoikilocytosis [ORDO Disease]
- Hereditary pyropoikilocytosis (disorder) [SNOMED CT concept]
- Piropoikilocytosis [PASCAL descriptor]
- Pyropoikilocytosis [HPO term]
- Pyropoikilocytosis, hereditary [OMIM Phenotype]
- hereditary pyropoikilocytosis [Disease (Nov.)]
- hereditary pyropoikilocytosis [SNOMED Notion]
HPO term
- Pyropoikilocytosis [HPO term]
MeSH term(s) associated for indexing
- elliptocytosis, hereditary [MeSH Descriptor]
Record concept(s)
- pyropoikilocytosis, hereditary [MeSH concept]
Semantic type(s)
- Disease or Syndrome [UMLS semantic type]
UMLS correspondences (same concept)
- Hereditary Pyropoikilocytosis [NCIt concept]
- Hereditary pyropoikilocytosis [ORDO Disease]
- Hereditary pyropoikilocytosis [ICD-11 More detail]
- Hereditary pyropoikilocytosis [MedDRA LLT]
- Hereditary pyropoikilocytosis (disorder) [SNOMED CT concept]
- Piropoikilocytosis [PASCAL descriptor]
- Pyropoikilocytosis [HPO term]
- Pyropoikilocytosis, hereditary [OMIM Phenotype]
- hereditary pyropoikilocytosis [SNOMED Notion]
- hereditary pyropoikilocytosis [Disease (Nov.)]