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lung mucinous cystadenocarcinoma
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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.] |
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signet ring lung adenocarcinoma
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DOID_0080305 |
[A lung adenocarcinoma containing a signet cell ring component characterized by abundant intracellular mucin accumulation and a displaced crescentic nucleus.] |
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acute dyspnea
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SYMP_0000679 |
[A dyspnea that is characterized by a severe and sudden onset.] |
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dyspnea
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SYMP_0019153 |
[A respiratory abnormality that is characterized by difficult or labored respiration.] |
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acute gastroenteritis
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SYMP_0000677 |
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acquired generalized lipodystrophy
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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.] |
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acute mental dysfunction
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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.] |
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atypical hemolytic-uremic syndrome
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DOID_0080301 |
[A complement deficiency that is characterized by mechanical hemolytic anemia, thrombocytopenia, and renal dysfunction.] |
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complement deficiency
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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.] |
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solid adenocarcinoma with mucin production
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DOID_0080306 |
[A lung adenocarcinoma that lacks acini, tubules, and papillae, and contains many mucin-containing cells.] |
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myofibrillar myopathy 8
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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.] |
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infantile-onset myofibrillar myopathy-2B
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DOID_0080309 |
[A myofibrillar myopathy that has_material_basis_in homozygous mutation in the CRYAB gene on chromosome 11q23.] |
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acute diarrhea
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SYMP_0000675 |
[Acute diarrhea is a diarrhea with either or both a rapid onset or a short course.] |
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acute enteritis
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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.] |
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neurofibromatosis
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DOID_8712 |
|
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bradykinesia
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SYMP_0000673 |
[Bradykinesia is a hypokinesia characterized by an extreme slowness in the execution of movements and reflexes.] |
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acute cranial nerve dysfunction
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SYMP_0000674 |
|
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obsolete carcinoma in situ of respiratory system
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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.] |
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sudden onset of fever
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SYMP_0000671 |
|
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decubitus ulcer
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DOID_8717 |
[A chronic ulcer of skin where the ulcer is an ulceration of tissue deprived of adequate blood supply by prolonged pressure.] |