Mitchell-Riley syndrome
human disease
Press Enter · cited answer in seconds
0 sources
Mitchell-Riley syndrome
Summary
Mitchell-Riley syndrome is a rare disease[1].
Key Facts
- Mitchell-Riley syndrome's instance of is recorded as rare disease[2].
- Mitchell-Riley syndrome's instance of is recorded as class of disease[3].
- Mitchell-Riley syndrome's subclass of is recorded as neonatal diabetes mellitus[4].
- Mitchell-Riley syndrome's subclass of is recorded as intestinal atresia[5].
- Mitchell-Riley syndrome's MeSH descriptor ID is recorded as C567570[6].
- Mitchell-Riley syndrome's OMIM ID is recorded as 615710[7].
- Mitchell-Riley syndrome's KEGG ID is recorded as H01377[8].
- Mitchell-Riley syndrome's Orphanet ID is recorded as 293864[9].
- Mitchell-Riley syndrome's genetic association is recorded as RFX6[10].
- Mitchell-Riley syndrome's Google Knowledge Graph ID is recorded as /g/11h557x1wy[11].
- Mitchell-Riley syndrome's exact match is recorded as http://www.orpha.net/ORDO/Orphanet_293864[12].
- Mitchell-Riley syndrome's UMLS CUI is recorded as C2748662[13].
- Mitchell-Riley syndrome's UMLS CUI is recorded as C4751130[14].
- Mitchell-Riley syndrome's ICD-10-CM is recorded as Q45.8[15].
- Mitchell-Riley syndrome's Mondo ID is recorded as MONDO_0014315[16].
- Mitchell-Riley syndrome's UniProt disease ID is recorded as DI-02515[17].