Undritz anomaly

Preferred Label : Undritz anomaly;

Type : Phenotype or locus, molecular basis unknown;

Alternative titles and symbols : Hypersegmentation of nuclei of polymorphonuclear leukocytes;

Inheritance : Autosomal dominant;

Prefixed ID : %191500;

Details

Origin ID

191500;

UMLS CUI

C1860604;

Currated CISMeF NLP mapping
- undritz anomaly [MeSH concept]
- undritz anomaly [MeSH Supplementary Concept]
HPO term(s)
- Autosomal dominant inheritance [HPO term]
- Hypersegmentation of neutrophil nuclei [HPO term]
Semantic type(s)
- Disease or Syndrome [UMLS semantic type]
UMLS correspondences (same concept)
- undritz anomaly [MeSH Supplementary Concept]
- undritz anomaly [MeSH concept]

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