Bruton-type agammaglobulinemia
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Bruton-type agammaglobulinemia
Summary
Bruton-type agammaglobulinemia is a hereditary disorder[1]. It has Wikipedia articles in 13 language editions, a strong signal of global cultural recognition.[2]
Key Facts
- Bruton-type agammaglobulinemia's instance of is recorded as hereditary disorder[3].
- Bruton-type agammaglobulinemia's instance of is recorded as rare disease[4].
- Bruton-type agammaglobulinemia's instance of is recorded as class of disease[5].
- Bruton-type agammaglobulinemia is a type of agammaglobulinemia[6].
- Bruton-type agammaglobulinemia is a type of X-linked recessive disease[7].
- Bruton-type agammaglobulinemia is a type of agammaglobulinemia[8].
- Bruton-type agammaglobulinemia's NCI Thesaurus ID is recorded as C3822[9].
- Bruton-type agammaglobulinemia's health specialty is recorded as immunology[10].
- Bruton-type agammaglobulinemia's genetic association is recorded as BTK[11].
- Bruton-type agammaglobulinemia's exact match is recorded as http://purl.obolibrary.org/obo/DOID_14179[12].
- Bruton-type agammaglobulinemia's exact match is recorded as http://identifiers.org/doid/DOID:14179[13].
- Bruton-type agammaglobulinemia's on focus list of Wikimedia project is recorded as WikiProject Medicine[14].
Why It Matters
Bruton-type agammaglobulinemia has Wikipedia articles in 13 language editions, a strong signal of global cultural recognition.[2] It is known by 19 alternative names across languages and contexts.[15]