Whim syndrome 2

Preferred Label : Whim syndrome 2;

Symbol : WHIMS2;

Type : Phenotype, molecular basis known;

Alternative titles and symbols : Warts, hypogammaglobulinemia, infections, and myelokathexis syndrome 2;

Prefixed ID : #619407;

Détails

Origin ID

619407;

UMLS CUI

C5543622;

Genes related to phenotype
- Chemokine, cxc motif, receptor 2 [OMIM gene]
HPO term(s)
- Autosomal recessive inheritance [HPO term]
- Chronic neutropenia [HPO term]
- Myelokathexis [HPO term]
Semantic type(s)
- Disease or Syndrome [UMLS semantic type]

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