Autosomal recessive combined immunodeficiency due to Arp2/3-mediated filament branching defect

Autosomal recessive combined immunodeficiency due to Arp2/3-mediated filament branching defect (disorder)

active

Code	`1351778007`
Semantic tag	disorder
Module	international
Definition	primitive
Effective time	20241201

Synonyms

Autosomal recessive combined immunodeficiency due to ARPC1B mutation

Parents (7)

85995004Autosomal recessive hereditary disorder disorder
442459007Combined immunodeficiency disease disorder
36138009Congenital immunodeficiency disease disorder
737221003Congenital thrombocytopaenia disorder
363138005Hereditary disorder of immune system disorder
438492008Hereditary thrombocytopenic disorder disorder
2897005Immune thrombocytopenia disorder

Children (0)

None (leaf concept).