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Summary Literature (0)
DOID:0110912 - leukocyte adhesion deficiency 3

Disease Ontology Definition:A leukocyte adhesion deficiency that is characterized by a defect in beta integrins 1, 2, and 3; which impairs the integrin activation cascade and has_material_basis_in mutation in FERMT3 gene on chromosome 11q12.

Synonyms: IADD, integrin activation deficiency disease, LAD1V, LAD1 variant, LAD3, leukocyte adhesion deficiency 1 variant, leukocyte adhesion deficiency type III

Xenbase Genes : fermt3

Mondo Disease Ontology (on Monarch Initiative):
MONDO:0013016 - leukocyte adhesion deficiency 3


Other Model Organisms: Alliance, MGI, ZFIN, FlyBase, WormBase, RGD

Ontology Viewers: Disease Ontology, EMBL-EBI, OLSVis tree view, Ontobee
Parent(s): leukocyte adhesion deficiency (is_a)