3308 (4.0%)
|
Beta-ketothiolase deficiency
---- α-メチルアセト酢酸尿症
|
不穏
常染色体劣性遺伝
A rare organic aciduria affecting ketone body metabolism and the catabolism of isoleucine and characterized by intermittent ketoacidotic episodes associated with vomiting, dyspnea, tachypnoea, hypotonia, lethargy and coma, with an onset during infancy or toddlerhood and usually ceasing by adolescence.
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Orphanet:134
日本語症例報告(J-STAGE & J-GLOBAL)
画像検索 (Google)
症例報告検索
Monarch
UR-DBMS
KEGG:H01076
|
3308 (4.0%)
|
Subacute sclerosing leukoencephalitis
|
ネフローゼ症候群
常染色体劣性遺伝
A chronic progressive encephalitis that develops a few years after measles infection and presents with a demyelination of the cerebral cortex.
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Orphanet:2806
日本語症例報告(J-STAGE & J-GLOBAL)
画像検索 (Google)
症例報告検索
Monarch
UR-DBMS
KEGG:H01696
|
3308 (4.0%)
|
Ornithine transcarbamylase deficiency
---- オルニチントランスカルバミラーゼ欠損症
|
盲
X連鎖劣性遺伝
Ornithine transcarbamylase deficiency (OTCD) is a disorder of urea cycle metabolism and ammonia detoxification (see this term) characterized by either a severe, neonatal-onset disease found almost exclusively in males, or later-onset (partial) forms of the disease. Both present with episodes of hyperammonemia that can be fatal and which can lead to neurological complications.
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Orphanet:664
日本語症例報告(J-STAGE & J-GLOBAL)
画像検索 (Google)
症例報告検索
Monarch
UR-DBMS
KEGG:H00187
Gene Reviews
|
3308 (4.0%)
|
Hyperornithinemia-hyperammonemia-homocitrullinuria syndrome
|
脈絡膜網膜萎縮
常染色体劣性遺伝
Hyperornithinemia-hyperammonemia-homocitrullinuria syndrome (triple H syndrome) is a disorder of urea cycle metabolism characterized by either a neonatal-onset with manifestations of lethargy, poor feeding, vomiting and tachypnea or, more commonly, presentations in infancy, childhood or adulthood with chronic neurocognitive deficits, acute encephalopathy and/or chronic liver dysfunction.
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Orphanet:415
日本語症例報告(J-STAGE & J-GLOBAL)
画像検索 (Google)
症例報告検索
Monarch
UR-DBMS
KEGG:H01268
Gene Reviews
|
3308 (4.0%)
|
Primary hepatic neuroendocrine carcinoma
|
眼瞼下垂
Primary hepatic neuroendocrine carcinoma (PHNEC) is a rare hepatic tumor that may manifest with abdominal pain or fullness, as well as diarrhea or weight loss. More than 10% of cases are asymptomatic and in rare cases a carcinoid syndrome may be observed.
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Orphanet:100085
日本語症例報告(J-STAGE & J-GLOBAL)
画像検索 (Google)
症例報告検索
Monarch
|
3308 (4.0%)
|
Intermediate uveitis
---- 中間部ぶどう膜炎
|
蛋白尿
Orphanet:279914
日本語症例報告(J-STAGE & J-GLOBAL)
画像検索 (Google)
症例報告検索
Monarch
|
3308 (4.0%)
|
Early-onset schizophrenia
|
行動異常
A rare, neurologic disease characterized by an early onset of positive and negative symptoms of psychosis that impact development and cognitive functioning. Clinical manifestation commonly include premorbid features of autism spectrum disorders, attention deficits, neurodevelopmental delays, and behavioral abnormalities. After the onset of psychotic symptoms, other comorbidities are also common, including obsessive-compulsive disorder, major depressive disorder, attention deficit hyperactivity disorder, expressive and receptive language disorders, auditory processing deficits, and executive functioning deficits.
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Orphanet:96369
日本語症例報告(J-STAGE & J-GLOBAL)
画像検索 (Google)
症例報告検索
Monarch
|
3308 (4.0%)
|
Mitochondrial DNA-associated Leigh syndrome
|
腎尿細管異常
Maternally inherited Leigh syndrome is a rare subtype of Leigh syndrome (see this term) characterized clinically by encephalopathy, lactic acidosis, seizures, cardiomyopathy, respiratory disorders and developmental delay, with onset in infancy or early childhood, and resulting from maternally-inherited mutations in mitochondrial DNA.
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Orphanet:255210
日本語症例報告(J-STAGE & J-GLOBAL)
画像検索 (Google)
症例報告検索
Monarch
|
3308 (4.0%)
|
VIPoma
---- VIP産生腫瘍
|
糖尿病
VIPoma is an extremely rare type of pancreatic neuroendocrine tumor (see this term) that secretes vasoactive intestinal polypeptide (VIP) leading to the manifestations of watery diarrhea, hypokalemia and achlorhydia or hypochhlorhydia (known as WDHA syndrome).
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Orphanet:97282
日本語症例報告(J-STAGE & J-GLOBAL)
画像検索 (Google)
症例報告検索
Monarch
|
3308 (4.0%)
|
Hypokalemic periodic paralysis
---- 低カリウム血症周期性麻痺1型
|
女性型乳房
A rare disorder characterised by episodes of muscle paralysis lasting from a few to 24-48 hours and associated with a fall in blood potassium levels.
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Orphanet:681
日本語症例報告(J-STAGE & J-GLOBAL)
画像検索 (Google)
症例報告検索
Monarch
|