3308 (4.0%)
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Fructose-1,6-bisphosphatase deficiency
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被刺激性
常染色体劣性遺伝
Fructose-1,6-biphosphatase (FBP) deficiency is a disorder of fructose metabolism (see this term) characterized by recurrent episodes of fasting hypoglycemia with lactic acidosis, that may be life-threatening in neonates and infants.
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Orphanet:348
日本語症例報告(J-STAGE & J-GLOBAL)
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Monarch
UR-DBMS
KEGG:H00114
|
3308 (4.0%)
|
Wells syndrome
|
黄疸
Wells syndrome is characterised by the presence of recurrent cellulitis-like eruptions with eosinophilia.
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Orphanet:901
日本語症例報告(J-STAGE & J-GLOBAL)
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Monarch
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3308 (4.0%)
|
Neuroendocrine tumor of stomach
|
全身疾患の皮膚症状
Gastric neuroendocrine tumor is a rare subtype of neuroendocrine neoplasm, arising from enterochromaffin-like cells in the stomach, with a variable clinical presentation, disease course and prognosis, depending on the disease type and histological grade. Most patients are asymptomatic, with diagnosis usually occurring incidentally during gastroscopy, however, symptoms of dyspepsia, anemia, pain, weight loss and gastrointestinal bleeding can be observed. Association with Zollinger-Ellison syndrome and multiple endocrine neoplasia type I has been reported.
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Orphanet:100075
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|
3308 (4.0%)
|
Acute fatty liver of pregnancy
---- 妊娠性急性脂肪肝
|
多尿
A rare, severe complication occurring in the third trimester of pregnancy or in early postpartum period bearing a risk for perinatal and maternal mortality and characterized by jaundice, rise of hepatic injuries and evolving to acute liver failure and encephalopathy.
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Orphanet:243367
日本語症例報告(J-STAGE & J-GLOBAL)
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Monarch
|
3308 (4.0%)
|
Plasma cell leukemia
---- 形質細胞性白血病
|
腎不全
Orphanet:454714
日本語症例報告(J-STAGE & J-GLOBAL)
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症例報告検索
Monarch
|
3308 (4.0%)
|
Adenohypophysitis
|
無月経
A rare, acquired pituitary hormone deficiency, a type of primary hypophysitis characterized by an inflammation of anterior pituitary. Clinical presentation is variable and includes headaches, visual disturbances, symptoms of adrenal insufficiency, hyperprolactinemia, hypothyroidism and hypogonadism. It most commonly affects young women during pregnancy or postpartum period.
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Orphanet:95512
日本語症例報告(J-STAGE & J-GLOBAL)
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症例報告検索
Monarch
|
3308 (4.0%)
|
Manganese poisoning
---- マンガン中毒
|
視力障害
Orphanet:306682
日本語症例報告(J-STAGE & J-GLOBAL)
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Monarch
|
3308 (4.0%)
|
Niemann-Pick disease type C
---- Niemann-Pick 病C型
|
垂直性核上性注視麻痺
Niemann-Pick disease type C (NP-C) is a lysosomal lipid storage disease (see this term) characterized by variable clinical signs, depending on the age of onset, such as prolonged unexplained neonatal jaundice or cholestasis, isolated unexplained splenomegaly, and progressive, often severe neurological symptoms such as cognitive decline, cerebellar ataxia, vertical supranuclear gaze palsy (VSPG), dysarthria, dysphagia, dystonia, seizures, gelastic cataplexy, and psychiatric disorders.
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Orphanet:646
日本語症例報告(J-STAGE & J-GLOBAL)
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Monarch
|
3308 (4.0%)
|
Lafora disease
---- ミオクロニーてんかん Lafora
|
盲
常染色体劣性遺伝
Heterogeneous
Lafora disease (LD) is a rare, inherited, severe, progressive myoclonic epilepsy characterized by myoclonus and/or generalized seizures, visual hallucinations (partial occipital seizures), and progressive neurological decline.
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Orphanet:501
日本語症例報告(J-STAGE & J-GLOBAL)
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症例報告検索
Monarch
UR-DBMS
KEGG:H01994
Gene Reviews
|
3308 (4.0%)
|
Long chain 3-hydroxyacyl-CoA dehydrogenase deficiency
|
網膜症
常染色体劣性遺伝
A mitochondrial disorder of long chain fatty acid oxidation characterized in most patients by onset in infancy/ early childhood of hypoketotic hypoglycemia, metabolic acidosis, liver disease, hypotonia and, frequently, cardiac involvement with arrhythmias and/or cardiomyopathy.
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Orphanet:5
日本語症例報告(J-STAGE & J-GLOBAL)
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症例報告検索
Monarch
UR-DBMS
KEGG:H00489
|