All terms in DOID

Label Id Description
Infantile onset HP_0003593 [Onset of signs or symptoms of disease between 28 days to one year of life.]
lymphoblastoma SYMP_0000084
lymphatic system symptom SYMP_0019141
obsolete Salmonella arizonae intestinal infectious disease DOID_10958 [A Salmonella infectious disease that involves infection of the intestine caused by Salmonella enterica subsp arizonae, which is a gut inhabitant of reptiles. The symptoms include fever, headache, abdominal pain, vomiting, and diarrhea.]
lesions in lung SYMP_0000082
obsolete Escherichia coli intestinal infectious disease DOID_10959 [A primary bacterial infectious disease that involves infection of the intestine by the bacterium Escherichia coli, caused by consumption of contaminated food and water. Some strains of Escherichia coli produce Shiga toxin, which cause severe illness. The symptoms include severe stomach cramps, fever, diarrhea (sometimes bloody), and vomiting.]
lymphangitis SYMP_0000083
obsolete Enterobacter aerogenes intestinal infectious disease DOID_10957 [An intestinal infectious disease that involves infection of the intestine by nosocomial bacterium Enterobacter aerogenes, which results in formation of ulcers.]
strongyloidiasis DOID_10955 [A parasitic helminthiasis infectious disease that involves infection of the intestine, lungs, skin and central nervous system with nematode Strongyloides stercoralis.]
parasitic helminthiasis infectious disease DOID_883 [A parasitic infectious disease that occurs when part of the body is infested with parasitic worms such as cestodes, nematodes and trematodes.]
adenosine deaminase deficiency DOID_5810 [A severe combined immunodeficiency that is caused by a defective enzyme, adenosine deaminase (ADA), necessary for the breakdown of purines. Lack of ADA causes accumulation of dATP.]
severe combined immunodeficiency DOID_627 [A combined T cell and B cell immunodeficiency that is caused by a defect in infection-fighting immune cells resulting in individuals with non-functional immune systems.]
MHC class II deficiency DOID_5812 [A severe combined immunodeficiency that is characterized by deficiency of MHC class II molecules that causes lack of immune protection against bacteria, viruses, and fungi and thus causes early death in childhood, and has_material_basis_in autosomal recessive inheritance of mutation in the CIITA, RFX5, RFXANK, and RFXAP genes.]
meningoencephalitis SYMP_0000089 [A nervous system symptom that is characterized by an inflammation of the brain and meninges.]
lymphopenia SYMP_0000086
purine nucleoside phosphorylase deficiency DOID_5813 [A combined T cell and B cell immunodeficiency that is a rare autosomal recessive metabolic disorder that has_material_basis_in mutation in the PNP gene and characterized mainly by decreased T-cell function.]
combined T cell and B cell immunodeficiency DOID_628 [A primary immunodeficiency disease characterized by impaired T cell-mediated immunity and impaired B cell mediated humoral immunity.]
massive hepatic necrosis SYMP_0000087
susceptibility to autism 7 MIM_610676
Lacazia NCBITaxon_121739