sialidosis
inherited metabolic disorder
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sialidosis
Summary
sialidosis is a developmental defect during embryogenesis[1].
Key Facts
- sialidosis's instance of is recorded as developmental defect during embryogenesis[2].
- sialidosis's instance of is recorded as class of disease[3].
- sialidosis's subclass of is recorded as oligosaccharidosis[4].
- sialidosis's KEGG ID is recorded as H00142[5].
- sialidosis's Orphanet ID is recorded as 309294[6].
- sialidosis's genetic association is recorded as NEU1[7].
- sialidosis's exact match is recorded as http://www.orpha.net/ORDO/Orphanet_309294[8].
- sialidosis's ICD-10-CM is recorded as E77.1[9].
- sialidosis's Mondo ID is recorded as MONDO_0017734[10].
- sialidosis's Genetics Home Reference Conditions ID is recorded as sialidosis[11].
- sialidosis's ICD-11 ID is recorded as 1180347697[12].
- sialidosis's UniProt disease ID is recorded as DI-02304[13].