All terms in DOID

Label Id Description
primary ovarian insufficiency 2B DOID_0080859 [A primary ovarian insufficiency that has_material_basis_in mutation in the POF1B gene.]
Rhamnaceae NCBITaxon_3608
obsolete childhood precursor T-lymphoblastic lymphoma/leukemia DOID_7933
obsolete recurrent malignant peritoneal mesothelioma DOID_6602
glandular-alveolar pattern testicular yolk sac tumor DOID_7930
obsolete old burn scar-related squamous cell carcinoma of skin DOID_7931
refractory T lymphoblastic leukemia/lymphoma DOID_7936
refractory hematologic cancer DOID_712 [A hematologic cancer that is located in the blood or bone marrow that doesn't respond to treatment.]
classic variant of chromophobe renal cell carcinoma DOID_6605
eosinophilic variant of chromophobe renal cell carcinoma DOID_6606
Kummell's disease DOID_6603
obsolete spondylosis and allied disorder DOID_6604
mixed astrocytoma-ependymoma DOID_7907
occupational asthma DOID_0080820 [An environmental induced asthma that is characterized by a variable airflow limitation due to exposure to inhaled irritants in the workplace.]
environmental induced asthma DOID_0080819 [An intrinsic asthma that is characterized by exposure to tobacco smoke and other inflammatory gases or particulate matter.]
exercise-induced bronchoconstriction DOID_0080821 [An intrinsic asthma that is characterized by narrowing of the airways during or shortly after exercise.]
intrinsic asthma DOID_9360 [A chronic asthma that is triggered by factors not attributable to allergies.]
aspirin-induced respiratory disease DOID_0080822 [An intrinsic asthma that is characterized by severe and prolonged airway obstruction after the ingestion of aspirin or other non-steroidal anti-inflammatory drugs.]
human cytomegalovirus infection DOID_0080827 [A viral infectious disease that has_material_basis_in Human betaherpesvirus 5 (Cytomegalovirus humanbeta5).]
VEXAS syndrome DOID_0080828 [A syndrome that is characterized by blood clots in veins, recurrent fevers, pulmonary abnormalities and vacuoles in myeloid cells and that has_material_basis_in mutation in the UBA1 gene on chromosome Xp11.]