Autosomal dominant hyperimmunoglobulin M syndrome due to AID deficiency

Autosomal dominant hyperimmunoglobulin M syndrome due to activation induced cytidine deaminase deficiency (disorder)

active

Code	`1351570003`
Semantic tag	disorder
Module	international
Definition	primitive
Effective time	20241101

Synonyms

Autosomal dominant activation-induced cytidine deaminase deficiency
Autosomal dominant hyper IgM syndrome due to AICDA
Autosomal dominant hyper-IgM syndrome type 2
Autosomal dominant hyperimmunoglobulin M syndrome due to activation induced cytidine deaminase deficiency

Parents (2)

11164009Autosomal dominant hereditary disorder disorder
783249007Hyperimmunoglobulin M syndrome without susceptibility to opportunistic infection disorder

Children (0)

None (leaf concept).