molybdenum cofactor deficiency |
Disease ID | 1398 |
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Disease | molybdenum cofactor deficiency |
Definition | Absence of molybdenum cofactor(2-), a cofactor for enzymes including sulfite oxidase, xanthine oxidoreductase, and aldehyde oxidase. [HPO:probinson] |
Synonym | combined molybdoflavoprotein enzyme deficiency combined molybdoflavoprotein enzyme deficiency (disorder) combined xanthine oxidase and aldehyde oxidase deficiency combined xanthine oxidase and aldehyde oxidase deficiency (disorder) combined xanthine oxidase and sulfite oxidase and aldehyde oxidase deficiency combined xanthine oxidase and sulphite oxidase and aldehyde oxidase deficiency deficiency of molybdenum cofactor hereditary xanthinuria type 2 hereditary xanthinuria, type 2 sulfite oxidase, xanthine dehydrogenase, and aldehyde oxidase, combined deficiency of xanthine oxidase-sulfite oxidase deficiency xanthine oxidase-sulphite oxidase deficiency |
OMIM | |
UMLS | C0268119 |
SNOMED-CT | |
Comorbidity | UMLS | Disease | Sentences' Count(Total Sentences:1) |
Curated Gene | Entrez_id | Symbol | Resource(Total Genes:3) |
Inferring Gene | (Waiting for update.) |
Text Mined Gene | (Waiting for update.) |
Locus | (Waiting for update.) |
Disease ID | 1398 |
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Disease | molybdenum cofactor deficiency |
Integrated Phenotype | (Waiting for update.) |
Text Mined Phenotype | HPO | Name | Sentences' Count(Total Phenotypes:3) |
Disease ID | 1398 |
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Disease | molybdenum cofactor deficiency |
Manually Symptom | UMLS | Name(Total Manually Symptoms:2) |
Text Mined Symptom | (Waiting for update.) |
Manually Genotype(Total Text Mining Genotypes:0) |
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All Snps(Total Genotypes:0) | |
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GWASdb Annotation(Total Genotypes:0) | |
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GWASdb Snp Trait(Total Genotypes:0) | |
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Mapped by lexical matching(Total Items:0) |
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Mapped by homologous gene(Total Items:0) |
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Chemical(Total Drugs:0) | |
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FDA approved drug and dosage information(Total Drugs:0) | |
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FDA labeling changes(Total Drugs:0) | |
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