microcephaly with chemotactic defect and transient hypogammaglobulinemia

Preferred Label : microcephaly with chemotactic defect and transient hypogammaglobulinemia;

Origin ID

C565381;

UMLS CUI

C1855078;

Currated CISMeF NLP mapping
- Microcephaly with chemotactic defect and transient hypogammaglobulinemia [OMIM Phenotype]
MeSH term(s) associated for indexing
- agammaglobulinemia [MeSH Descriptor]
- facies [MeSH Descriptor]
- microcephaly [MeSH Descriptor]
Record concept(s)
- microcephaly with chemotactic defect and transient hypogammaglobulinemia [MeSH concept]
Semantic type(s)
- Disease or Syndrome [UMLS semantic type]
UMLS correspondences (same concept)
- Microcephaly with chemotactic defect and transient hypogammaglobulinemia [OMIM Phenotype]