Autosomal recessive hyperimmunoglobulin M syndrome due to CTNNBL1 deficiency

Autosomal recessive hyperimmunoglobulin M syndrome due to catenin beta like 1deficiency (disorder)

active

Code	`1351575008`
Semantic tag	disorder
Module	international
Definition	primitive
Effective time	20241101

Synonyms

Autosomal recessive hyperimmunoglobulin M syndrome due to catenin beta like 1deficiency
Hyper IgM syndrome due to CTNNBL1

Parents (1)

403836001Autosomal recessive hyperimmunoglobulin M syndrome disorder

Children (0)

None (leaf concept).