Disease Information for Hyperammonemia, hereditary

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Clinical Manifestations
Signs & Symptoms
Meat intolerance
Lethargy/torpor
Clinical Presentation & Variations
Presentation/Metabolic disease silent first week Missed
Presentation/Non diabetic Ketoacidosis Kids infants
Presentation/Progressive dementia Child Infant
Disease Progression
Course/Chronic disorder
Course/Chronic only
Demographics & Risk Factors
Population Group
Child
Population/Pediatrics population
Sex & Age Groups
Population/Child
Population/Child-Infant Only
Population/Children/all
Laboratory Tests
Abnormal Lab Findings (Non Measured)
Filter paper spot/newborn blood test abnormal
Newborn screening tests abnormal (extended)
Abnormal Lab Findings - Decreased
BUN/Creatinine ratio (Lab)
Abnormal Lab Findings - Increased
Ammonia blood (Lab)
URINE Ammonia
Associated Diseases & Rule outs
Associated Disease & Complications
CNS disease/involvement
Coma in Children
Developmental neurologic degeneration/child
Encephalopathy/CNS effect
Hyperammonemia
Disease Mechanism & Classification
Class
CLASS/Pediatric disorders (ex)
Pathophysiology
Pathophysiology/Gene locus 13q14
Pathophysiology/Gene locus Chromosome 13
Pathophysiology/Gene Locus Identified/OMIM database
Pathophysiology/Genomic indentifiers (polymorphism/snip/mutations)
Process
PROCESS/Biochemical (category)
PROCESS/Hereditofamilial (category)
Definition
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External Links Related to Hyperammonemia, hereditary
Google
Wikipedia
Merck
Images
PubMed (National Library of Medicine)
NGC (National Guideline Clearinghouse)
Medscape (eMedicine)
Harrison's Online (accessmedicine)
NEJM (The New England Journal of Medicine)
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