dihydropyrimidinuria
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dihydropyrimidinuria
Summary
dihydropyrimidinuria is a class of disease[1].
Key Facts
- dihydropyrimidinuria's instance of is recorded as class of disease[2].
- dihydropyrimidinuria's subclass of is recorded as dihydropyrimidine dehydrogenase deficiency[3].
- dihydropyrimidinuria's OMIM ID is recorded as 222748[4].
- dihydropyrimidinuria's KEGG ID is recorded as H00199[5].
- dihydropyrimidinuria's Orphanet ID is recorded as 38874[6].
- dihydropyrimidinuria's ICD-9-CM is recorded as 277.2[7].
- dihydropyrimidinuria's genetic association is recorded as DPYS[8].
- dihydropyrimidinuria's exact match is recorded as http://www.orpha.net/ORDO/Orphanet_38874[9].
- dihydropyrimidinuria's UMLS CUI is recorded as C0342803[10].
- dihydropyrimidinuria's UMLS CUI is recorded as C3495551[11].
- dihydropyrimidinuria's ICD-10-CM is recorded as E79.8[12].
- dihydropyrimidinuria's GARD rare disease ID is recorded as 12347[13].
- dihydropyrimidinuria's Mondo ID is recorded as MONDO_0009111[14].
- dihydropyrimidinuria's UniProt disease ID is recorded as DI-01483[15].