All terms in DOID

Label Id Description
autoimmune disease of the nervous system DOID_438 [An autoimmune disease affecting the nervous system.]
obsolete Hodgkin's lymphoma, nodular sclerosis, involving intrapelvic lymph nodes DOID_9130
Hepacivirus hominis NCBITaxon_3052230
obsolete Intraventricular hemorrhage from any perinatal cause DOID_433
obsolete Hodgkin's lymphoma, lymphocytic depletion, involving intra-abdominal lymph nodes DOID_9124
eczema herpeticum DOID_9123 [A herpes simplex that results_in infection located_in skin, effected by preexisting dermatosis, has_material_basis_in Human herpesvirus 1 (Simplexvirus humanalpha1) or 2 (Simplexvirus humanalpha2). The infection has_symptom watery blisters, has_symptom fever, and has_symptom swelling of the lymph nodes.]
myofascial pain syndrome DOID_431
obsolete Hodgkin's lymphoma, mixed cellularity, extranodal and solid organ sites DOID_9121
myasthenia gravis DOID_437 [An autoimmune disease of the nervous system that has_material_basis_in antibodies to acetylcholine receptors at the neuromuscular junction, has_symptom ptosis, has_symptom diplopia, has_symptom dysphagia, has_symptom dysarthria, has_symptom muscle weakness and has_symptom shortness of breath.]
posterior mediastinum cancer DOID_436
hydrazide CHEBI_35362
obsolete malignant neoplasm of thymus, heart and mediastinum DOID_435
obsolete anterior mediastinum cancer DOID_434
tooth-like structure UBERON_0003913
lower gum cancer DOID_9125
homocarnosinosis DOID_0060177 [A gamma-amino butyric acid metabolism disorder that is characterized by an excess of homocarnosine in the brain and has_material_basis_in a deficiency of serum carnosinase in its ability to hydrolyze homocarnosine.]
gamma-amino butyric acid metabolism disorder DOID_0060176 [An amino acid metabolic disorder characterized by impairment of the GABA catabolic pathway.]
succinic semialdehyde dehydrogenase deficiency DOID_0060175 [A gamma-amino butyric acid metabolism disorder that is characterized by a deficiency of succinic semialdehyde dehydrogenase resulting in elevated levels of gamma-hydroxybutyric acid.]
glioma susceptibility 4 MIM_607248
GABA aminotransferase deficiency DOID_0060174 [A gamma-amino butyric acid metabolism disorder that is characterized by a defect in the gene coding for gamma-aminobutyrate transaminase, which is responsible for catabolism of gamma-aminobutyric acid (GABA), an important, mostly inhibitory neurotransmitter in the central nervous system, into succinic semialdehyde.]