All terms in DOID

Label Id Description
lung mucinous cystadenocarcinoma DOID_0080304 [A lung adenocarcinoma that is a very rare malignant mucus-producing neoplasm arising from the uncontrolled growth of transformed epithelial cells originating in lung tissue.]
signet ring lung adenocarcinoma DOID_0080305 [A lung adenocarcinoma containing a signet cell ring component characterized by abundant intracellular mucin accumulation and a displaced crescentic nucleus.]
acute dyspnea SYMP_0000679 [A dyspnea that is characterized by a severe and sudden onset.]
dyspnea SYMP_0019153 [A respiratory abnormality that is characterized by difficult or labored respiration.]
acute gastroenteritis SYMP_0000677
acquired generalized lipodystrophy DOID_0080300 [A complete generalized lipodystrophy that is characterized by generalized disappearance of fat occurring during childhood and adolescence where normal body fat is present at birth.]
acute mental dysfunction SYMP_0000678 [A nervous system symptom that is characterized by a severe and sudden onset of disturbance in the normal operation of one's cognition, emotional regulation, or behaviour.]
atypical hemolytic-uremic syndrome DOID_0080301 [A complement deficiency that is characterized by mechanical hemolytic anemia, thrombocytopenia, and renal dysfunction.]
complement deficiency DOID_626 [A primary immunodeficiency disease that is the result in a mutation of a gene encoding one of the thirty complement system proteins, produced predominantly in liver, which function to defend against infection and produce inflammation.]
solid adenocarcinoma with mucin production DOID_0080306 [A lung adenocarcinoma that lacks acini, tubules, and papillae, and contains many mucin-containing cells.]
myofibrillar myopathy 8 DOID_0080308 [A myofibrillar myopathy that is characterized by childhood onset of slowly progressive proximal muscle weakness and atrophy resulting in increased falls, gait problems, and difficulty running or climbing stairs, and has_material_basis_in autosomal recessive inheritance of homozygous or compound heterozygous mutation in the PYROXD1 gene on chromosome 12p12.]
infantile-onset myofibrillar myopathy-2B DOID_0080309 [A myofibrillar myopathy that has_material_basis_in homozygous mutation in the CRYAB gene on chromosome 11q23.]
acute diarrhea SYMP_0000675 [Acute diarrhea is a diarrhea with either or both a rapid onset or a short course.]
acute enteritis SYMP_0000676 [Acute enteritis is a enteritis with either or both a rapid onset and a short course which is usually due to bacteria or virus.]
neurofibromatosis DOID_8712
bradykinesia SYMP_0000673 [Bradykinesia is a hypokinesia characterized by an extreme slowness in the execution of movements and reflexes.]
acute cranial nerve dysfunction SYMP_0000674
obsolete carcinoma in situ of respiratory system DOID_8718 [A carcinoma in situ that is characterized by the spread of cancer in the respiratory system and the lack of invasion of surrounding tissues.]
sudden onset of fever SYMP_0000671
decubitus ulcer DOID_8717 [A chronic ulcer of skin where the ulcer is an ulceration of tissue deprived of adequate blood supply by prolonged pressure.]