Infantile free sialic acid storage disease
human disease
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Infantile free sialic acid storage disease
Summary
Infantile free sialic acid storage disease is a rare disease[1].
Key Facts
- Infantile free sialic acid storage disease's instance of is recorded as rare disease[2].
- Infantile free sialic acid storage disease's instance of is recorded as class of disease[3].
- Infantile free sialic acid storage disease's subclass of is recorded as sialuria[4].
- Infantile free sialic acid storage disease's OMIM ID is recorded as 269920[5].
- Infantile free sialic acid storage disease's Orphanet ID is recorded as 309324[6].
- Infantile free sialic acid storage disease's genetic association is recorded as SLC17A5[7].
- Infantile free sialic acid storage disease's exact match is recorded as http://www.orpha.net/ORDO/Orphanet_309324[8].
- Infantile free sialic acid storage disease's exact match is recorded as http://www.orpha.net/ORDO/Orphanet_834[9].
- Infantile free sialic acid storage disease's UMLS CUI is recorded as C1963905[10].
- Infantile free sialic acid storage disease's UMLS CUI is recorded as C2930923[11].
- Infantile free sialic acid storage disease's UMLS CUI is recorded as C1096902[12].
- Infantile free sialic acid storage disease's ICD-10-CM is recorded as E77.8[13].
- Infantile free sialic acid storage disease's GARD rare disease ID is recorded as 175[14].
- Infantile free sialic acid storage disease's Mondo ID is recorded as MONDO_0010027[15].
- Infantile free sialic acid storage disease's Microsoft Academic ID is recorded as 2778975676[16].
- Infantile free sialic acid storage disease's WikiProjectMed ID is recorded as Infantile free sialic acid storage disease[17].
- Infantile free sialic acid storage disease's UniProt disease ID is recorded as DI-01820[18].