Rabson–Mendenhall syndrome

Summary

Rabson–Mendenhall syndrome is a rare disease^[1]. It draws 17 Wikipedia views per month (rare_disease category, ranking #226 of 627).^[2]

Key Facts

• Rabson–Mendenhall syndrome's instance of is recorded as rare disease^[3].
• Rabson–Mendenhall syndrome's instance of is recorded as class of disease^[4].
• S.M. Rabson is named after Rabson–Mendenhall syndrome^[5].
• E. N. Mendenhall is named after Rabson–Mendenhall syndrome^[6].
• Rabson–Mendenhall syndrome's subclass of is recorded as Donohue syndrome^[7].
• Rabson–Mendenhall syndrome's OMIM ID is recorded as 262190^[8].
• Rabson–Mendenhall syndrome's ICD-10 ID is recorded as E13^[9].
• Rabson–Mendenhall syndrome's Freebase ID is recorded as /m/02px1t_^[10].
• Rabson–Mendenhall syndrome's KEGG ID is recorded as H00942^[11].
• Rabson–Mendenhall syndrome's Orphanet ID is recorded as 769^[12].
• Rabson–Mendenhall syndrome's health specialty is recorded as endocrinology^[13].
• Rabson–Mendenhall syndrome's genetic association is recorded as INSR^[14].
• Rabson–Mendenhall syndrome's UMLS CUI is recorded as C0271695^[15].
• Rabson–Mendenhall syndrome's Medical Dictionary for Regulatory Activities ID is recorded as 10012601^[16].
• Rabson–Mendenhall syndrome's GARD rare disease ID is recorded as 226^[17].
• Rabson–Mendenhall syndrome's Mondo ID is recorded as MONDO_0009874^[18].
• Rabson–Mendenhall syndrome's Microsoft Academic ID is recorded as 2777630319^[19].
• Rabson–Mendenhall syndrome's Genetics Home Reference Conditions ID is recorded as rabson-mendenhall-syndrome^[20].
• Rabson–Mendenhall syndrome's WikiProjectMed ID is recorded as Rabson–Mendenhall syndrome^[21].
• Rabson–Mendenhall syndrome's UniProt disease ID is recorded as DI-02242^[22].

Why It Matters

Rabson–Mendenhall syndrome draws 17 Wikipedia views per month (rare_disease category, ranking #226 of 627).^[2] It has Wikipedia articles in 7 language editions, a strong signal of global cultural recognition.^[23]