All terms in DOID

Label Id Description
obsolete pulmonary syphilis DOID_11097 [A tertiary syphilis that is caused by the spirochetal bacterium Treponema pallidum subspecies pallidum. It is a sexually transmitted disease although congenital syphilis can also occur. Treponema infection of the lung leads to a fibrous induration spreading from the roots of the lungs. Ulcerations occur in the superficial tissues, while in the deep tissues gummata are formed. Symptoms include dry cough, hemoptysis, hemorrhage, dyspnea, pain in the chest, loss of weight and slight fever.]
melanocyte CL_0000148
pigment cell CL_0000147
obsolete Salmonella gastroenteritis DOID_11092 [A Salmonella infectious disease that involves inflammation of the stomach and intestines caused by Salmonella infection. The symptoms include diarrhea, vomiting, abdominal pain, fever and weakness.]
obsolete bacterial gastroenteritis DOID_11093 [A gastroenteritis that involves inflammation of the stomach and intestines caused by bacteria. The symptoms include abdominal cramps and pain, diarrhea, loss of appetite, nausea, and vomiting.]
obsolete idiopathic generalized epilepsy 15 DOID_0111316 [An idiopathic generalized epilepsy that has_material_basis_in heterozygous mutation in the RORB on chromosome 9q21.13.]
obsolete idiopathic generalized epilepsy 2 DOID_0111317 [An idiopathic generalized epilepsy that has_material_basis_in variation in a region on chromosome 14q23.]
obsolete idiopathic generalized epilepsy 13 DOID_0111314 [An idiopathic generalized epilepsy that has_material_basis_in heterozygous mutation in the GABRA1 on chromosome 5q34.]
obsolete idiopathic generalized epilepsy 14 DOID_0111315 [An idiopathic generalized epilepsy that has_material_basis_in heterozygous mutation in the SLC12A5 on chromosome 20q13.12.]
obsolete idiopathic generalized epilepsy 11 DOID_0111312 [An idiopathic generalized epilepsy that has_material_basis_in heterozygous mutation in the CLCN2 on chromosome 3q27.1.]
obsolete idiopathic generalized epilepsy 12 DOID_0111313 [An idiopathic generalized epilepsy that has_material_basis_in heterozygous mutation in the SLC2A1 on chromosome 1p34.2.]
familial febrile seizures 2 DOID_0111310 [A familial febrile seizures that has_material_basis_in variation in a region on chromosome 19p13.3.]
familial febrile seizures DOID_0111297 [A brain disease characterized by seizures during childhood associated with febrile episodes without any evidence of intracranial infection or defined pathologic or traumatic cause with a familial pattern of inheritance.]
familial febrile seizures 7 DOID_0111311 [A familial febrile seizures that has_material_basis_in heterozygous mutation.]
obsolete idiopathic generalized epilepsy 3 DOID_0111318 [An idiopathic generalized epilepsy that has_material_basis_in variation in a region on chromosome 9q32-q33.]
obsolete idiopathic generalized epilepsy 4 DOID_0111319 [An idiopathic generalized epilepsy that has_material_basis_in variation in a region on chromosome 10q25-q26.]
mercury CHEBI_25195 [A heavy metal that is mercury, is toxic to living organisms, is an odorless, shiny, silver-white liquid that is commonly used in thermometers, barometers and fluorescent light bulbs.]
carbohydrate secreting cell CL_0000447
familial febrile seizures 4 DOID_0111305 [A familial febrile seizures that has_material_basis_in heterozygous mutation the ADGRV1 gene on chromosome 5q14.3.]
familial febrile seizures 5 DOID_0111306 [A familial febrile seizures that has_material_basis_in variation in a region on chromosome 6q22-q24.]