Leukocyte nuclear appendages, hereditary prevalence of

Preferred Label : Leukocyte nuclear appendages, hereditary prevalence of;

Type : Other, mainly phenotypes with suspected mendelian basis;

Inheritance : Autosomal dominant;

Prefixed ID : 151500;

Details

Origin ID

151500;

UMLS CUI

C1835405;

Currated CISMeF NLP mapping
- leukocyte nuclear appendages, hereditary prevalence of [MeSH concept]
- leukocyte nuclear appendages, hereditary prevalence of [MeSH Supplementary Concept]
HPO term(s)
- Abnormality of blood and blood-forming tissues [HPO term]
- Autosomal dominant inheritance [HPO term]
Semantic type(s)
- Disease or Syndrome [UMLS semantic type]
UMLS correspondences (same concept)
- leukocyte nuclear appendages, hereditary prevalence of [MeSH Supplementary Concept]
- leukocyte nuclear appendages, hereditary prevalence of [MeSH concept]

Keyword's position in hierarchy(ies) :

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