Autosomal recessive hyperimmunoglobulin M syndrome due to MSH6 deficiency

Autosomal recessive hyperimmunoglobulin M syndrome due to mutator S homolog 6 deficiency (disorder)

active
Code1351576009
Semantic tagdisorder
Moduleinternational
Definitionprimitive
Effective time20241101

Synonyms

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None (leaf concept).