hyperammonemia

medical condition
rdfs:label
"hyperammonemia"@en
skos:altLabel "高氨血症"@zh
"高血氨症"@zh
schema:description
"medical condition"@en
schema:dateModified "2026-07-11T13:58:16+00:00"^^xsd:dateTime
schema:version 2516280677
wikibase:identifiers 21
24
wikibase:sitelinks 19
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p:direct-normalized/P4527 <http://data.parliament.uk/terms/450160>
p:direct-normalized/P486 <http://id.nlm.nih.gov/mesh/D022124>
p:direct-normalized/P6366 <https://makg.org/entity/2781099255>
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p:direct-normalized/P672 <http://id.nlm.nih.gov/mesh/C23.550.421>
wdt:P10283 "C2781099255"
wdt:P10565 "133357"
"51607"
wdt:P11143 "Hyperammonemia"
wdt:P1343 Brockhaus and Efron Encyclopedic Dictionary
wdt:P1417 "science/hyperammonemia"
wdt:P14541 "JzdmE"
"bm69N"
wdt:P1542 somnolence
coma
intellectual disability
disorientation
ataxia
irritability
apathy
neurotoxicity
death
attention span
situation awareness
hyperventilation
encephalopathy
seizure
asterixis
gait abnormality
grunting
cerebral edema
wdt:P1552 abnormally high value
wdt:P1748 "C98950"
wdt:P1995 endocrinology
wdt:P279 amino acid metabolic disorder
wdt:P2888 <http://purl.obolibrary.org/obo/HP_0001987>
wdt:P2892 "C0220994"
wdt:P31 metabolic disease
abnormally high value
wdt:P373 "Hyperammonemia"
wdt:P3827 "hyperammonemia"
wdt:P3841 "HP:0001987"
wdt:P4527 "450160"
wdt:P486 "D022124"
wdt:P493 "270.6"
wdt:P494 "E72.2"
wdt:P557 "20468"
wdt:P6366 "2781099255"
"2911207822"
wdt:P646 "/m/02p0x7"
wdt:P6706 "iperammoniemìa"
wdt:P672 "C23.550.421"
wdt:P673 "1174503"
"944996"
wdt:P780 vomiting
lethargy
slurred speech
mental confusion
headache
wdt:P7807 "1920867021"
wdt:P828 hepatotoxicity
argininosuccinic aciduria
portal vein thrombosis
cystic fibrosis
viral hepatitis
topiramate
valproic acid
Congenital lactic acidosis
sulfadiazine
asphyxia neonatorum
ornithine carbamoyltransferase deficiency
neonatal herpes simplex
klebsiellosis
isovaleric acidemia
carbamazepin
Escherichia coli infectious disease
multiple myeloma
carbamoyl phosphate synthetase I deficiency disease
chronic hepatitis C
chronic hepatitis B
acyl-CoA dehydrogenase deficiency
salicylate
ischemic hepatitis
alpha-1-antitrypsin deficiency
biliary atresia
Reye syndrome
argininemia
acute leukemia
wdt:P924 β-lactulose
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