Immunodeficiency 99 with hypogammaglobulinemia and autoimmune cytopenias

Preferred Label : Immunodeficiency 99 with hypogammaglobulinemia and autoimmune cytopenias;

Symbol : IMD99;

Type : Phenotype, molecular basis known;

Prefixed ID : #619846;

Details

Origin ID

619846;

UMLS CUI

C5676971;

Genes related to phenotype
- Catenin, beta-like, 1 [OMIM gene]
Semantic type(s)
- Disease or Syndrome [UMLS semantic type]

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