Ayazi syndrome

Summary

Ayazi syndrome is a class of disease^[1]. It draws 3 Wikipedia views per month (class_of_disease category, ranking #630 of 1,968).^[2]

Key Facts

• Ayazi syndrome's instance of is recorded as class of disease^[3].
• Ayazi syndrome's subclass of is recorded as choroideremia^[4].
• Ayazi syndrome's subclass of is recorded as syndromic obesity^[5].
• Ayazi syndrome's subclass of is recorded as hereditary retinal dystrophy^[6].
• Ayazi syndrome's subclass of is recorded as syndromic genetic deafness^[7].
• Ayazi syndrome's subclass of is recorded as unclassified familial retinal dystrophy^[8].
• Ayazi syndrome's subclass of is recorded as partial deletion of the long arm of chromosome X^[9].
• Ayazi syndrome's subclass of is recorded as head and neck disease^[10].
• Ayazi syndrome's subclass of is recorded as developmental defect during embryogenesis^[11].
• Ayazi syndrome's MeSH descriptor ID is recorded as C537793^[12].
• Ayazi syndrome's OMIM ID is recorded as 303110^[13].
• Ayazi syndrome's Orphanet ID is recorded as 1435^[14].
• Ayazi syndrome's exact match is recorded as http://www.orpha.net/ORDO/Orphanet_1435^[15].
• Ayazi syndrome's UMLS CUI is recorded as C3551019^[16].
• Ayazi syndrome's UMLS CUI is recorded as C1844836^[17].
• Ayazi syndrome's Quora topic ID is recorded as Ayazi-Syndrome^[18].
• Ayazi syndrome's ICD-10-CM is recorded as Q87.8^[19].
• Ayazi syndrome's GARD rare disease ID is recorded as 369^[20].
• Ayazi syndrome's Mondo ID is recorded as MONDO_0010558^[21].
• Ayazi syndrome's SNOMED CT ID is recorded as 717761005^[22].

Why It Matters

Ayazi syndrome draws 3 Wikipedia views per month (class_of_disease category, ranking #630 of 1,968).^[2] It is known by 6 alternative names across languages and contexts.^[23]