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autosomal agammaglobulinemia

Go to external page http://purl.obolibrary.org/obo/MONDO_0011096

Agammaglobulinemia, non-Bruton type (autosomal agammaglobulinemia) is a rare form of agammaglobulinemia, a primary immunodeficiency disease, and is characterized by variable immune dysfunction with frequent and recurrent bacterial infections and/or chronic diarrhea. [ Orphanet:33110 ]

Synonyms: agammaglobulinemia, non-Bruton type AGM autosomal agammaglobulinemia

This is just here as a test because I lose it

Term information

database cross reference
  • GARD:9640 (Orphanet:33110)
  • MESH:C538056 (MONDO:equivalentTo)
  • UMLS:C1832241 (Orphanet:33110)
  • Orphanet:33110 (OMIM:601495)
Subsets

gard_rare, ordo_clinical_subtype, rare, nord_rare, orphanet_rare, clingen

exactMatch

http://linkedlifedata.com/resource/umls/id/C1832241

http://www.orpha.net/ORDO/Orphanet_33110

http://identifiers.org/mesh/C538056

has related synonym

agammaglobulinemia, autosomal recessive, due to IGHM defect

id

MONDO:0011096

seeAlso

https://search.clinicalgenome.org/kb/conditions/MONDO:0011096

Term relations