MOMO syndrome

Summary

MOMO syndrome is a rare disease^[1]. It draws 20 Wikipedia views per month (rare_disease category, ranking #219 of 627).^[2]

Key Facts

• MOMO syndrome's instance of is recorded as rare disease^[3].
• MOMO syndrome's instance of is recorded as developmental defect during embryogenesis^[4].
• MOMO syndrome's instance of is recorded as class of disease^[5].
• MOMO syndrome's subclass of is recorded as syndromic obesity^[6].
• MOMO syndrome's MeSH descriptor ID is recorded as C535812^[7].
• MOMO syndrome's OMIM ID is recorded as 157980^[8].
• MOMO syndrome's Freebase ID is recorded as /m/069ggv^[9].
• MOMO syndrome's symptoms and signs is recorded as obesity^[10].
• MOMO syndrome's symptoms and signs is recorded as macrocephaly^[11].
• MOMO syndrome's symptoms and signs is recorded as intellectual disability^[12].
• MOMO syndrome's symptoms and signs is recorded as eye disease^[13].
• MOMO syndrome's Orphanet ID is recorded as 2563^[14].
• MOMO syndrome's health specialty is recorded as genetics^[15].
• MOMO syndrome's UMLS CUI is recorded as C1834759^[16].
• MOMO syndrome's ICD-10-CM is recorded as Q87.3^[17].
• MOMO syndrome's GARD rare disease ID is recorded as 178^[18].
• MOMO syndrome's Mondo ID is recorded as MONDO_0008008^[19].
• MOMO syndrome's Microsoft Academic ID is recorded as 2777901294^[20].
• MOMO syndrome's ICD-11 ID is recorded as 348695820^[21].
• MOMO syndrome's WikiProjectMed ID is recorded as MOMO syndrome^[22].

Why It Matters

MOMO syndrome draws 20 Wikipedia views per month (rare_disease category, ranking #219 of 627).^[2] It has Wikipedia articles in 6 language editions, a strong signal of global cultural recognition.^[23] It is known by 8 alternative names across languages and contexts.^[24]