Agammaglobulinemia 8b, autosomal recessive

Preferred Label : Agammaglobulinemia 8b, autosomal recessive;

Symbol : AGM8B;

Type : Phenotype, molecular basis known;

Alternative titles and symbols : Agammaglobulinemia, autosomal recessive, due to tcf3 defect;

Prefixed ID : #619824;

Details

Origin ID

619824;

UMLS CUI

C5676958;

Genes related to phenotype
- Transcription factor 3 [OMIM gene]
ORDO concept(s)
- Autosomal agammaglobulinemia [ORDO Disease]
Semantic type(s)
- Disease or Syndrome [UMLS semantic type]

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