All terms in DOID

Label Id Description
dry beriberi DOID_0070318 [A beriberi that is located_in the nervous system and has_symptom difficulty walking, numbness in extremities, tingling in extremities, paralysis of lower legs, difficulty speaking, confusion, and vomiting.]
miliaria pustulosa DOID_0070319 [A miliaria that is characterized by pustules resulting from inflammation and bacterial infection.]
Fusobacteriia NCBITaxon_203490
Osteolysis HP_0002797
Abnormal bone structure HP_0003330
Paslahepevirus balayani NCBITaxon_1678143
edema SYMP_0000538 [A skin and integumentary tissue symptom that is characterized by an abnormal excess accumulation of serous fluid in connective tissue or in a serous cavity.]
jaundice SYMP_0000539 [A skin and integumentary tissue symptom that is characterized by a yellowish pigmentation of the skin, tissues, and certain body fluids is caused by the deposition of bile pigments that follows interference with normal production and discharge of bile (as in certain liver diseases) or excessive breakdown of red blood cells (as after internal hemorrhage or in various hemolytic states).]
disturbance of skin sensation SYMP_0000536
Abnormal pattern of respiration HP_0002793
Abnormal respiratory system physiology HP_0002795
cyanosis SYMP_0000537 [A skin and integumentary tissue symptom that is characterized by a bluish or purplish discoloration (as of skin) due to deficient oxygenation of the blood.]
spontaneous ecchymoses SYMP_0000534 [A skin and integumentary tissue symptom that is characterized by the spontaneous escape of blood into the tissues from ruptured blood vessels marked by a livid black-and-blue or purple spot or area.]
Blastomyces parvus NCBITaxon_2060905
Blastomyces NCBITaxon_229219
Abnormality of the respiratory system HP_0002086
change in skin texture SYMP_0000535
Abnormality of the uterus HP_0000130
Abnormal morphology of female internal genitalia HP_0000008
hypomyelinating leukodystrophy 17 DOID_0070404 [A hypomyelinating leukodystrophy characterized by onset in early infancy of microcephaly and lack of overall development that has_material_basis_in homozygous mutation in the AIMP2 gene on chromosome 7p22.]