Autosomal recessive combined immunodeficiency due to MAN2B2 mutation

Autosomal recessive combined immunodeficiency due to mannosidase alpha class 2B member 2 mutation (disorder)

active
Code1351946008
Semantic tagdisorder
Moduleinternational
Definitionprimitive
Effective time20241201

Synonyms

Parents (2)

Children (0)

None (leaf concept).