All terms in DOID

Label Id Description
Eurotiomycetidae NCBITaxon_451871
nasal cavity adenocarcinoma DOID_4930 [A nasal cavity carcinoma that derives_from epithelial cells of glandular origin.]
nasal cavity carcinoma DOID_4931 [A nasal cavity cancer that has_material_basis_in epithelial cells.]
ampulla of Vater carcinoma DOID_4932 [An ampulla of Vater cancer that has_material_basis_in abnormally proliferating cells derives_from epithelial cells.]
nasal cavity cancer DOID_10811 [A respiratory system cancer that is located_in the nasal cavity.]
apocrine sweat gland cancer DOID_4934
toxic encephalopathy DOID_3602 [A nervous system disease that results from exposure to neurotoxicants and is characterized by an altered mental status, memory loss, and visual problems.]
mucinous cystadenocarcinoma DOID_3603 [A cystadenocarcinoma that derives_from epithelial cells originating in glandular tissue, with a capsulated structure and mucus-producing cells.]
apocrine carcinoma DOID_4933 [An apocrine sweat gland cancer that derives_from epithelial cells of glandular origin.]
infiltrating angiolipoma DOID_3615 [An angiolipoma that is characterized by prominent vascularity that invades the surrounding deep tissue.]
angiolipoma DOID_3616 [A lipoma that is a painful subcutaneous nodule, having all other features of a typical lipoma.]
epidural spinal canal angiolipoma DOID_3617
epidural spinal canal neoplasm DOID_3618
major affective disorder 5 MIM_611535
acute retinal necrosis syndrome DOID_3611
retinitis DOID_3612
adenocarcinoma in situ DOID_4943 [An in situ carcinoma that derives_from epithelial cells of glandular origin.]
in situ carcinoma DOID_8719 [A carcinoma that is an early development defined by the absence of invasion of surrounding tissues.]
obsolete combined hepatocellular carcinoma and cholangiocarcinoma DOID_4942
Canavan disease DOID_3613 [A leukodystrophy characterized by onset in early infancy, atonia of neck muscles, hypotonia, hyperextension of legs and flexion of arms, blindness, severe mental defect, megalocephaly, and death by 18 months on the average that has_material_basis_in homozygous or compound heterozygous mutation in ASPA gene encoding aspartoacylase on chromosome 17p13.]