All terms in DOID

Label Id Description
ehrlichiosis DOID_10242 [A primary bacterial infectious disease that results in infection located_in leukocyte, has_material_basis_in Ehrlichia chaffeensis or Anaplasma phagocytophilum, which are transmitted_by lone star tick and transmitted_by black-legged tick respectively. The infection has_symptom headache, has_symptom muscle aches, has_symptom fatigue and has_symptom rash.]
listeriosis DOID_11573 [A primary bacterial infectious disease that results_in infection, has_material_basis_in Listeria monocytogenes, which is transmitted_by ingestion of contaminated food or raw milk or transmitted_by congenital method. Ingestion of Listeria by pregnant women has_symptom nausea, has_symptom vomiting, has_symptom diarrhea, has_symptom fever, has_symptom malaise, has_symptom back pain, and has_symptom headache. Maternal infection with Listeria can result in chorioamnionitis, premature labor, spontaneous abortion, or stillbirth.]
gallbladder leiomyoma DOID_5140 [A gastrointestinal system benign neoplasm that is located_in the gallbladder and derives_from smooth muscle cells.]
vulvar leiomyoma DOID_5142 [A vulvar benign neoplasm that is located_in smooth muscle cells.]
clear cell variant infiltrating bladder urothelial carcinoma DOID_6476
large bowel leiomyoma DOID_5143 [An intestinal benign neoplasm that derives_from smooth muscle cells and that is located_in the large bowel.]
childhood teratocarcinoma of the testis DOID_6474
childhood testicular mixed germ cell tumor DOID_6161
appendix leiomyoma DOID_5146 [A gastrointestinal system benign neoplasm that derives_from smooth muscle cells and that is located_in the appendix.]
appendix disease DOID_60000 [A gastrointestinal system disease that is located_in the appendix.]
dartoic leiomyoma DOID_5147 [A reproductive organ benign neoplasm that has_material_basis_in the dartos muscle located_in the scrotum or labia majora.]
hyperimmunoglobulinemia D periodic fever syndrome DOID_0081450 [A hyperimmunoglobulin syndrome that is characterized as periodic fever from early infancy accompanied by elevated serum C-reactive protein and that has_material_basis_in homozygous or compound heterozygous mutation in the gene encoding mevalonate kinase (MVK) on chromosome 12q24.]
hyperimmunoglobulin syndrome DOID_2959 [A B cell deficiency that is characterized by relative predominance of certain immunoglobulin subtypes and deficiencies of others.]
PFAPA syndrome DOID_0081451 [An autoimmune disease that is characterized by recurrent febrile episodes associated with aphthous stomatitis, pharyngitis and cervical adenitis.]
mitochondrial DNA depletion syndrome 2 DOID_0080120 [A mitochondrial DNA depletion syndrome that is characterized by childhood onset of muscle weakness associated with depletion of mtDNA in skeletal muscle, and has_material_basis_in autosomal recessive inheritance of homozygous or compound heterozygous mutation in the mitochondrial thymidine kinase gene on chromosome 16q21.]
epithelioid neurofibroma DOID_5149
mitochondrial DNA depletion syndrome 3 DOID_0080121 [A mitochondrial DNA depletion syndrome that is characterized by onset in infancy of progressive liver failure and neurologic abnormalities, hypoglycemia, and increased lactate in body fluids, and has_material_basis_in autosomal recessive inheritance of homozygous or compound heterozygous mutation in the deoxyguanosine kinase gene on chromosome 2p13.]
Iris coloboma HP_0000612
Coloboma HP_0000589
Abnormality iris morphology HP_0000525