All terms in DOID

Label Id Description
acute myeloid leukemia with mutated NPM1 DOID_0081089 [An acute myeloid leukemia with mutation of the nucleophosmin gene. It is usually associated with normal karyotype and frequently has myelomonocytic or monocytic features.]
acute myelomonocytic leukemia DOID_0081082 [An acute myeloid leukemia that is characterized by the proliferation of both neutrophil and monocyte precursors.]
acute myeloid leukemia with inv(3) (q21.3;q26.2) or t(3;3) (q21.3;q26.2) DOID_0081083 [An acute myeloid leukemia associated with inv(3)(q21q26.2) or t(3;3)(q21;q26.2), resulting in the expression of RPN1-EVI1 fusion protein and the reposition of a distal GATA2 enhancer to activate MECOM expression.]
acute myeloid leukemia with inv(16)(p13.1q22) or t(16;16)(p13.1;q22) DOID_0081084 [An acute myeloid leukemia that is characterized by the presence of abnormal bone marrow eosinophils and the characteristic cytogenetic abnormality inv(16)(p13.1q22) or t(16;16)(p13.1;q22), which results in the expression of the fusion protein CBFB-MYH11.]
acute myeloid leukemia with minimal differentiation DOID_0081085 [An acute myeloid leukemia in which the blasts do not show evidence of myeloid differentiation by morphology and conventional cytochemistry.]
obsolete AIDS-related vulvovaginal candidiasis DOID_2503 [A vulvovaginal candidiasis that involves fungal infection of the vaginal mucous membranes by Candida albicans in AIDS patients.]
Crigler-Najjar syndrome DOID_3803 [A bilirubin metabolic disorder that involves a build up of bilirubin as bilirubin is not being broken down as a result of a lack or deficiency of the enzyme uridine diphosphate glycosyltransferase (UGT).]
bilirubin metabolic disorder DOID_2741 [An inherited metabolic disorder that involves elevated levels of bilirubin resulting from disruption of bilirubin metabolism.]
porokeratosis DOID_3805
gestational diabetes insipidus DOID_0081057 [A diabetes insipidus that is characterized by progressively rising levels of placental vasopressinase throughout pregnancy, resulting in decreased endogenous vasopressin and resulting hypotonic polyuria worsening through the pregnancy.]
diabetes insipidus DOID_9409 [A kidney disease that is characterized by polydipsia and polyuria with a dilute urine having a specific gravity less than 1.010, hypernatremia, and dehydration.]
dipsogenic diabetes insipidus DOID_0081058 [A diabetes insipidus that is characterized by excessive thirst, polyuria with low urine osmolality, and intact urine concentrating ability.]
X-linked central diabetes insipidus DOID_0081059 [A central diabetes insipidus that has_material_basis_in X-linked inheritance.]
central diabetes insipidus DOID_0081055 [A diabetes insipidus that is characterized by polyuria and polydipsia due to a deficiency in vasopressin synthesis.]
epidural spinal canal meningioma DOID_3809
spinal canal and spinal cord meningioma DOID_1140
endocrine system disease DOID_28 [A disease of anatomical entity that is located_in endocrine glands which secretes a type of hormone directly into the bloodstream to regulate the body.]
disease of anatomical entity DOID_7 [A disease that manifests in a defined anatomical structure.]
Molluscipoxvirus NCBITaxon_10278
Chordopoxvirinae NCBITaxon_10241