neutropenia, severe congenital, autosomal dominant 2

Preferred Label : neutropenia, severe congenital, autosomal dominant 2;

MeSH note : GFI1 mutations;

MeSH synonym : severe congenital Neutropenia-2;

Détails

Origin ID

C567748;

UMLS CUI

C2751288;

Currated CISMeF NLP mapping
- Neutropenia, severe congenital, 2, autosomal dominant [OMIM Phenotype]
- Severe Congenital Neutropenia Type 2, Autosomal Dominant [NCIt concept]
MeSH term(s) associated for indexing
- neutropenia [MeSH Descriptor]
Record concept(s)
- neutropenia, severe congenital, autosomal dominant 2 [MeSH concept]
Semantic type(s)
- Disease or Syndrome [UMLS semantic type]
UMLS correspondences (same concept)
- Neutropenia, severe congenital, 2, autosomal dominant [OMIM Phenotype]
- Severe Congenital Neutropenia Type 2, Autosomal Dominant [NCIt concept]

Position du mot-clé dans l'(les) arborescence(s) :

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