Neu-Laxova syndrome

Summary

Neu-Laxova syndrome is a class of disease^[1]. It draws 94 Wikipedia views per month (class_of_disease category, ranking #551 of 1,968).^[2]

Key Facts

• Neu-Laxova syndrome's instance of is recorded as class of disease^[3].
• Richard L. Neu is named after Neu-Laxova syndrome^[4].
• Neu-Laxova syndrome's subclass of is recorded as 3-phosphoglycerate dehydrogenase deficiency^[5].
• Neu-Laxova syndrome's Commons category is recorded as Neu-Laxova syndrome^[6].
• Neu-Laxova syndrome's MeSH descriptor ID is recorded as C536405^[7].
• Neu-Laxova syndrome's OMIM ID is recorded as 256520^[8].
• Neu-Laxova syndrome's KEGG ID is recorded as H02117^[9].
• Neu-Laxova syndrome's Orphanet ID is recorded as 2671^[10].
• Neu-Laxova syndrome's health specialty is recorded as medical genetics^[11].
• Neu-Laxova syndrome's UMLS CUI is recorded as C0265218^[12].
• Neu-Laxova syndrome's GARD rare disease ID is recorded as 102^[13].
• Neu-Laxova syndrome's Microsoft Academic ID is recorded as 2781181935^[14].
• Neu-Laxova syndrome's ICD-11 ID is recorded as 893358230^[15].
• Neu-Laxova syndrome's WikiProjectMed ID is recorded as Neu–Laxova syndrome^[16].

Why It Matters

Neu-Laxova syndrome draws 94 Wikipedia views per month (class_of_disease category, ranking #551 of 1,968).^[2] It has Wikipedia articles in 9 language editions, a strong signal of global cultural recognition.^[17] It is known by 3 alternative names across languages and contexts.^[18]