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- Disease Information
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Disease Processes ▼
- Auto Immune
- Vascular-Arteriosclerosis
- Biochemical
- Congenital-developmental
- Deficiency
- Degenrative-Necrosis
- Electromagnetic-Physics
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Major Organs-Systems ▼
- Systemic
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Disease Information for Ornithine Transcarbamylase (OTC) defic.: Disease Mechanism & Classification
- Clinical Manifestations (42)
- Demographics & Risk Factors (9)
- Laboratory Tests (13)
- Diagnostic Test Results (4)
- Associated Diseases & Rule outs (18)
- Disease Mechanism & Classification (25)
- Treatment (10)
- Synonyms
- Definition
- External Links Related to Ornithine Transcarbamylase (OTC) defic.
- Class
- CLASS/Pediatric disorders (ex)
- Pathophysiology
- Pathophysiology/Early defect urea cycle
- Pathophysiology/Gene locus 11p21.1
- Pathophysiology/Gene locus Chromosome X.
- Pathophysiology/Genomic indentifiers (polymorphism/snip/mutations)
- Pathophysiology/Heterozygous females/X-link/effected
- Pathophysiology/Homozygous/dominant lethal
- Pathophysiology/Maternal inheritance
- Pathophysiology/Single gene locus indentified
- Pathophysiology/Urea cycle metabolic defect
- Pathophysiology/Lethal Mutation Homozygous
- Pathophysiology/Lethal Mutation Males
- Pathophysiology/Lyon Hypothesis X Linked
- Pathophysiology/Mitochondrial lesion
- Process
- PROCESS/Aminoacid metabolic disorder (ex)
- PROCESS/Aminoaciduria (ex)
- PROCESS/Enzyme defect/Metabolic disorder (ex)
- PROCESS/Episodic disorder (ex)
- PROCESS/Genetic disorder/Spontaneous mutations/sporadic
- PROCESS/Hereditofamilial (category)
- PROCESS/INCIDENCE/Rare disease (ex)
- PROCESS/Metabolic/storage disorder (category)
- PROCESS/Sex-linked (X-linked) recessive inheritance (ex)
- PROCESS/X-Linked dominant inheritance (ex)
- PROCESS/Mitochondrial disorders (ex)
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