All terms in DOID

Label Id Description
muscular dystrophy DOID_9884 [A myopathy is characterized by progressive skeletal muscle weakness degeneration.]
antidepressant type abuse DOID_11718 [A substance abuse that involves the recurring use of antidepressant drugs despite negative consequences.]
Spermatophyta NCBITaxon_58024
diabetes mellitus DOID_9351 [A glucose metabolism disease that is characterized by chronic hyperglycaemia with disturbances of carbohydrate, fat and protein metabolism resulting from defects in insulin secretion, insulin action, or both.]
prediabetes syndrome DOID_11716 [A glucose metabolism disease that is characterized by blood glucose levels are high, but not high enough to be classified as type 2 diabetes.]
gestational diabetes DOID_11714 [A diabetes mellitus that manifests during pregnancy.]
diabetic angiopathy DOID_11713 [A peripheral vascular disease that is characterized by narrowing of the arteries as a complication arising from chronic diabetes.]
peripheral vascular disease DOID_341 [A vascular disease that is characterized by obstruction of vessels not within the coronary, aortic arch vasculature, or brain.]
Duchenne muscular dystrophy DOID_11723 [A muscular dystrophy that has_material_basis_in X-linked mutations in the DMD gene found on the X chromosome. It is characterized by rapidly progressing muscle weakness and muscle atrophy initially involving the lower extremities and eventually affecting the whole body. It affects males whereas females can be carriers. The symptoms start before the age of six and may appear at infancy.]
myotonic dystrophy type 1 DOID_11722 [A myotonic disease that is characterized by progressive muscle wasting and weakness affecting the distal skeletal and smooth muscles of lower legs, hands, neck, and face along with myotonia and cataracts and has_material_basis_in the autosomal dominant inheritance of the DMPK gene containing an expansion of a CTG trinucleotide repeat in the non-coding region.]
myotonic disease DOID_450 [A muscular dystrophy that is characterized by progressive muscle wasting and weakness.]
glycogen storage disease VII DOID_11721 [A glycogen storage disease that is characterized by exercise intolerance, muscle cramping, exertional myopathy, and compensated hemolysis and that has_material_basis_in homozygous or compound heterozygous mutation in the PFKM gene, which encodes muscle phosphofructokinase, on chromosome 12q13.]
Lyme disease DOID_11729 [A primary bacterial infectious disease that results_in infection, has_material_basis_in Borrelia burgdorferi, which is transmitted_by blacklegged tick (Ixodes scapularis) or transmitted_by western blacklegged tick (Ixodes pacificus). The infection has_symptom fever, has_symptom headache, has_symptom fatigue, and has_symptom skin rash called erythema migrans. If left untreated, infection can spread to joints, the heart, and the nervous system.]
limb-girdle muscular dystrophy DOID_11724 [A muscular dystrophy that is characterized by weakening of the muscles of the hip and shoulders which comprise the limb girdle muscles.]
obsolete syphilitic pericarditis DOID_11734
obsolete syphilitic aortic aneurysm DOID_11733
obsolete syphilitic myocarditis DOID_11732
gonococcal seminal vesiculitis DOID_10400
vesiculitis DOID_9365
gonorrhea DOID_7551 [A primary bacterial infectious disease that is a sexually transmitted infection, located_in uterus, located_in fallopian tube, located_in urethra, located_in mouth, located_in throat, located_in eye or located_in anus, has_material_basis_in Neisseria gonorrhoeae, which is transmitted_by contact with the penis, vagina, mouth, or anus or transmitted_by congenitally from mother to baby during delivery. The infection has_symptom burning sensation during urination, has_symptom discharge from the penis, has_symptom increased vaginal discharge, or has_symptom vaginal bleeding between periods.]