| IBED | Inter-African Bureau for Epizootic Diseases |
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| ICDA | International Classification of Diseases, Adapted |
| ICD-9-CM | International Classification of Diseases-ninth revision-Clinical Modification |
| ICD-10 | International Statistical Classification of Diseases and Health-related Problems, 10th revision |
| ICD-O | International Classification of Diseases-Oncology |
| lymphatic diseases | Diseases of lymph or lymph vessels. (12 Dec 1998) |
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| lysosomal diseases | Diseases (also called storage diseases) in which a deficiency of a particular lysosomal enzyme leads to accumulation of the undigested substrate for that enzyme within cells. Not immediately fatal, but within a few years lead to serious neurological and skeletal disorders and eventually to death. See: the following conditions: Hurler sundrome, Hunter syndrome, San Fillipo, Gaucher's disease, Niemann-Pick, Pompe's disease, Tay Sachs disease. (18 Nov 1997) |
| lysosomal storage diseases | Inborn errors of metabolism characterised by defects in specific lysosomal hydrolases and resulting in intracellular accumulation of unmetabolised substrates. (12 Dec 1998) |