All terms in DOID

Label Id Description
blastema predominant kidney Wilms' tumor DOID_5182
Sjogren's syndrome DOID_12894 [An autoimmune disease that involves attack of immune cells which destroy the exocrine glands that produce tears and saliva.]
autoimmune disease of exocrine system DOID_0060029 [An autoimmune disease that is the abnormal functioning of the immune system that causes your immune system to produce antibodies or T cells against cells and/or tissues in the exocrine system.]
retinal vasculitis DOID_11563 [A vasculitis that is characterized by inflammation of the vascular branches of the retinal artery and has_symptom painless decrease of visual acuity, visual floaters, dark spot in vision, decreased ability to distinguish colors, and distortion of images such as linear images.]
endometrium carcinoma in situ DOID_5172 [An in situ carcinoma that is located_in the endometrium.]
endometriosis DOID_289 [A female reproductive system disease characterized by the growth of endometrial tissue outside the uterine body.]
renal Wilms' tumor DOID_5176
mixed cell type kidney Wilms' tumor DOID_5179
obsolete malignant neoplasm of pelvic bones, sacrum and coccyx DOID_10239
metachronous kidney Wilms' tumor DOID_5178
medium chain acyl-CoA dehydrogenase deficiency DOID_0080153 [A lipid metabolism disorder that is characterized by a deficiency of the enzyme medium chain acyl-CoA dehydrogenase that results in the inability to convert medium chain fatty acids to energy, particularly during fasting.]
short chain acyl-CoA dehydrogenase deficiency DOID_0080154 [A lipid metabolism disorder that is characterized by deficiency of the enzyme short chain acyl-CoA dehydrogenase that results in the inability to convert short chain fatty acids.]
adrenocorticotropic hormone deficiency DOID_0080150 [A hypopituitarrium that is characterized by a decreased or absent production of adrenocorticotropic hormone by the pituitary gland.]
obsolete malignant neoplasm of pelvis DOID_10240
Listeria meningitis DOID_11572 [A bacterial meningitis that has_material_basis_in Listeria monocytogenes infection.]
mitochondrial DNA depletion syndrome 7 DOID_0080126 [A mitochondrial DNA depletion syndrome that is characterized by progressive ataxia, hypotonia, hyporeflexia, athetosis and sensory impairment and has_material_basis_in autosomal recessive homozygous or compound heterozygous mutation in the C10ORF2 gene, which encodes the twinkle and twinky proteins, on chromosome 10q24.]
intrathyroid thymic carcinoma DOID_0081457 [A thyroid gland carcinoma composed of groups of carcinoma cells with thymic epithelial differentiation.]
thyroid gland cribriform morular carcinoma DOID_0081458 [A thyroid gland carcinoma that is characterized by the presence of cribriform, trabecular, follicular, papillary, and solid growth patterns and squamoid morulae formation.]
mitochondrial DNA depletion syndrome 8a DOID_0080127 [A mitochondrial DNA depletion syndrome that is characterized by neonatal hypotonia, lactic acidosis, and neurologic deterioration, and has_material_basis_in autosomal recessive inheritance of homozygous or compound heterozygous mutation in the ribonucleotide reductase regulatory TP53 inducible subunit M2B gene on chromosome 8q22.]
Abnormal choroid morphology HP_0000610