isolated sulfite oxidase deficiency
human disease
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Summary
isolated sulfite oxidase deficiency is a developmental defect during embryogenesis[1]. It is known by 5 alternative names across languages and contexts.[2]
Key Facts
- isolated sulfite oxidase deficiency's instance of is recorded as developmental defect during embryogenesis[3].
- isolated sulfite oxidase deficiency's instance of is recorded as rare disease[4].
- isolated sulfite oxidase deficiency's instance of is recorded as class of disease[5].
- isolated sulfite oxidase deficiency is a type of encephalopathy due to sulfite oxidase deficiency[6].
- isolated sulfite oxidase deficiency is a type of autosomal recessive disease[7].
- isolated sulfite oxidase deficiency is a type of inherited metabolic disorder[8].
- isolated sulfite oxidase deficiency's genetic association is recorded as SUOX[9].
- isolated sulfite oxidase deficiency's exact match is recorded as http://purl.obolibrary.org/obo/HP_0003643[10].
- isolated sulfite oxidase deficiency's exact match is recorded as http://www.orpha.net/ORDO/Orphanet_833[11].
- isolated sulfite oxidase deficiency's exact match is recorded as http://www.orpha.net/ORDO/Orphanet_99731[12].
- isolated sulfite oxidase deficiency's exact match is recorded as http://purl.obolibrary.org/obo/DOID_0111270[13].
- isolated sulfite oxidase deficiency's exact match is recorded as http://identifiers.org/doid/DOID:0111270[14].
Why It Matters
isolated sulfite oxidase deficiency is known by 5 alternative names across languages and contexts.[2]