Autosomal recessive hyperimmunoglobulin M syndrome due to INO80 deficiency

Autosomal recessive hyperimmunoglobulin M syndrome due to INO80 complex ATPase subunit deficiency (disorder)

active

Code	`1351577000`
Semantic tag	disorder
Module	international
Definition	primitive
Effective time	20241101

Synonyms

Autosomal recessive hyperimmunoglobulin M syndrome due to INO80 complex ATPase subunit deficiency
Hyper IgM syndrome due to INO80

Parents (1)

403836001Autosomal recessive hyperimmunoglobulin M syndrome disorder

Children (0)

None (leaf concept).