All terms in DOID

Label Id Description
mild fever SYMP_0000881 [A fever that is characterized by being mild in form.]
Alzheimer's disease 1 DOID_0080348 [An Alzheimer's disease that has_material_basis_in mutation heterozygous mutation in the APP gene, which encodes the amyloid precursor protein, on chromosome 21q21.]
Alzheimer's disease DOID_10652 [A tauopathy that is characterized by memory lapses, confusion, emotional instability and progressive loss of mental ability and results in progressive memory loss, impaired thinking, disorientation, and changes in personality and mood starting and leads in advanced cases to a profound decline in cognitive and physical functioning and is marked histologically by the degeneration of brain neurons especially in the cerebral cortex and by the presence of neurofibrillary tangles and plaques containing beta-amyloid.]
developmental and epileptic encephalopathy 39 DOID_0080349 [A developmental and epileptic encephalopathy characterized by global developmental delay apparent in early infancy, early-onset seizures, hypotonia, poor motor function, and hypomyelination in the brain that has_material_basis_in mutation in the SLC25A12 gene on chromosome 2q31.]
decreased tongue tone SYMP_0000877
Simpson-Golabi-Behmel syndrome type 2 DOID_0080342 [A syndrome that has_material_basis_in mutation in the OFD1 gene on chromosome Xp22 and is characterized by developmental delay, macrocephaly, and respiratory problems.]
transient fever SYMP_0000878 [A fever that is characterized by a rise of body temperature above the normal that is sustained for only a short period of time.]
autosomal recessive pyridoxine-refractory sideroblastic anemia 3 DOID_0080343 [A sideroblastic anemia that is characterized by homozygous or compound heterozygous mutation in the GLRX5 gene on chromosome 14q32.]
Mus musculus NCBITaxon_10090
Mus <subgenus> NCBITaxon_862507
lameness SYMP_0000875 [Lameness is a musculoskeletal system symptom where a person is physically disabled as the result of having a body part and especially a limb so disabled as to impair freedom of movement.]
pericardial effusion SYMP_0000876 [Pericardial effusion is a cardiovascular system symptom where there is an abnormal accumulation of fluid in the pericardial cavity.]
blepharocheilodontic syndrome 1 DOID_0080345 [A blepharocheilodontic syndrome that has_material_basis_in heterozygous mutation in the CDH1 gene on chromosome 16q22.]
obsolete Hodgkin's lymphoma, nodular sclerosis, extranodal and solid organ sites DOID_8871
obsolete nodular lymphoma involving intrathoracic lymph nodes DOID_8870
breast apocrine adenoma DOID_7540 [A breast adenoma that is characterized by apocine differentiation.]
breast adenoma DOID_1625 [A breast benign neoplasm that is has_material_basis_in epithelial tissue in which tumor cells form glands or glandlike structures.]
ovarian endometrial cancer DOID_6212 [An ovary epithelial cancer that has_material_basis_in the endometrium and is located_in the ovary.]
obsolete recurrent squamous cell carcinoma of the esophagus DOID_7543
obsolete Hodgkin's sarcoma involving lymph nodes of multiple sites DOID_8875