Keppen–Lubinsky syndrome

Summary

Keppen–Lubinsky syndrome is a rare disease^[1]. It draws 3 Wikipedia views per month (rare_disease category, ranking #237 of 627).^[2]

Key Facts

• Keppen–Lubinsky syndrome's instance of is recorded as rare disease^[3].
• Keppen–Lubinsky syndrome's instance of is recorded as class of disease^[4].
• Keppen–Lubinsky syndrome's subclass of is recorded as genetic lipodystrophy^[5].
• Keppen–Lubinsky syndrome's OMIM ID is recorded as 614098^[6].
• Keppen–Lubinsky syndrome's Freebase ID is recorded as /m/0408xk9^[7].
• Keppen–Lubinsky syndrome's KEGG ID is recorded as H02236^[8].
• Keppen–Lubinsky syndrome's Orphanet ID is recorded as 435628^[9].
• Keppen–Lubinsky syndrome's genetic association is recorded as KCNJ6^[10].
• Keppen–Lubinsky syndrome's exact match is recorded as http://www.orpha.net/ORDO/Orphanet_435628^[11].
• Keppen–Lubinsky syndrome's UMLS CUI is recorded as C3279800^[12].
• Keppen–Lubinsky syndrome's ICD-10-CM is recorded as E88.1^[13].
• Keppen–Lubinsky syndrome's Mondo ID is recorded as MONDO_0013572^[14].
• Keppen–Lubinsky syndrome's UniProt disease ID is recorded as DI-04375^[15].

Why It Matters

Keppen–Lubinsky syndrome draws 3 Wikipedia views per month (rare_disease category, ranking #237 of 627).^[2]