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  2. Hyper-IgM syndrome type 2

Hyper-IgM syndrome type 2

Disease Export to PDF
Name:
Hyper-IgM syndrome type 2
ORPHAcode:
101089
Synonyms:
AID deficiency
Activation-induced cytidine deaminase deficiency
HIGM2
XREF(s):
Orphanet
ICD-10
OMIM
Analyte(s):
AICDA
Created:
13 May 2019 - 01:02
Changed:
22 Jun 2023 - 16:14