All terms in DOID

Label Id Description
sarcoid meningitis DOID_12055
Fanconi anemia complementation group D1 DOID_0111089 [A Fanconi anemia that has_material_basis_in homozygous or compound heterozygous mutation in the BRCA2 gene on chromosome 13q13.]
obsolete Trypanosoma meningitis DOID_12054 [A trypanosomiasis that involves inflammation of the meninges caused due to Trypanosoma species.]
Fanconi anemia complementation group G DOID_0111086 [A Fanconi anemia that has_material_basis_in homozygous or compound heterozygous mutation in the XRCC9 gene on chromosome 9p13.]
cryptococcosis DOID_12053 [An opportunistic mycosis that results_in fungal infection and has_material_basis_in Cryptococcus neoformans or Cryptococcus gattii.]
Fanconi anemia complementation group C DOID_0111087 [A Fanconi anemia that has_material_basis_in homozygous or compound heterozygous mutation in the FANCC gene on chromosome 9q22.]
obsolete cryptococcal meningitis DOID_12052 [A cryptococcosis that results_in inflammation located_in meninges, has_material_basis_in Cryptococcus neoformans and has_symptom headache, has_symptom nausea, has_symptom staggering gait, has_symptom dementia, has_symptom blurred vision and has_symptom confusion.]
Fanconi anemia complementation group E DOID_0111084 [A Fanconi anemia that has_material_basis_in homozygous mutation in the FANCE gene on chromosome 6p22-p21.]
megaloblastic anemia DOID_13382 [A macrocytic anemia that is characterized by inhibition of DNA synthesis during red blood cell production.]
Fanconi anemia complementation group U DOID_0111085 [A Fanconi anemia that has_material_basis_in homozygous mutation in the XRCC2 gene on chromosome 7q36.]
pernicious anemia DOID_13381 [A nutritional deficiency disease that is characterized by a decrease in red blood cells due to malabsorption of vitamin B12, has_symptom fatigue, pallor, shortness of breath, glossitis, ataxia, and/or paresthesia, has_material_basis_in atrophic gastritis, autoimmune disorder affecting the production or function of intrinsic factor, and/or genetic factors.]
Fanconi anemia complementation group L DOID_0111082 [A Fanconi anemia that has_material_basis_in homozygous or compound heterozygous mutation in the PHF9 gene on chromosome 2p16.]
obsolete acute pyelonephritis with lesion of renal medullary necrosis DOID_13380
Fanconi anemia complementation group D2 DOID_0111083 [A Fanconi anemia that has_material_basis_in compound heterozygous or homozygous mutation in the FANCD2 gene on chromosome 3p25.]
Oligoryzomys longicaudatus NCBITaxon_137207
Oligoryzomys NCBITaxon_29120
obsolete Fetal-maternal hemorrhage affecting management of mother DOID_12058
labia majora carcinoma DOID_13389 [A vulva carcinoma that is located_in the labia majora.]
Fanconi anemia complementation group I DOID_0111091 [A Fanconi anemia that has_material_basis_in homozygous or compound heterozygous mutation in the FANCI gene on chromosome 15q26.]
Fanconi anemia complementation group P DOID_0111092 [A Fanconi anemia characterized by increased chromosomal instability, progressive bone marrow failure and in some cases skeletal abnormalities that has_material_basis_in homozygous or compound heterozygous mutation in the SLX4 gene on chromosome 16p13.3.]