Barber-Say syndrome

Summary

Barber-Say syndrome is a developmental defect during embryogenesis^[1]. It draws 154 Wikipedia views per month (developmental_defect_during_embryogenesis category, ranking #39 of 308).^[2]

Key Facts

• Barber-Say syndrome's instance of is recorded as developmental defect during embryogenesis^[3].
• Barber-Say syndrome's instance of is recorded as rare disease^[4].
• Barber-Say syndrome's instance of is recorded as class of disease^[5].
• Barber-Say syndrome's subclass of is recorded as ectodermal dysplasia^[6].
• Barber-Say syndrome's subclass of is recorded as syndrome^[7].
• Barber-Say syndrome's subclass of is recorded as hypertrichosis of eyelid^[8].
• Barber-Say syndrome's subclass of is recorded as secondary ectropion^[9].
• Barber-Say syndrome's subclass of is recorded as microblepharon-ablephara syndrome^[10].
• Barber-Say syndrome's subclass of is recorded as congenital entropion^[11].
• Barber-Say syndrome's subclass of is recorded as syndromic developmental defect of the eye^[12].
• Barber-Say syndrome's subclass of is recorded as multiple congenital anomalies/dysmorphic syndrome without intellectual disability^[13].
• Barber-Say syndrome's MeSH descriptor ID is recorded as C537908^[14].
• Barber-Say syndrome's OMIM ID is recorded as 209885^[15].
• Barber-Say syndrome's DiseasesDB is recorded as 33294^[16].
• Barber-Say syndrome's KEGG ID is recorded as H01934^[17].
• Barber-Say syndrome's Disease Ontology ID is recorded as DOID:0060549^[18].
• Barber-Say syndrome's Orphanet ID is recorded as 1231^[19].
• Barber-Say syndrome's genetic association is recorded as TWIST2^[20].
• Barber-Say syndrome's Google Knowledge Graph ID is recorded as /g/11b6gspm6b^[21].
• Barber-Say syndrome's exact match is recorded as http://purl.obolibrary.org/obo/DOID_0060549^[22].
• Barber-Say syndrome's exact match is recorded as http://identifiers.org/doid/DOID:0060549^[23].
• Barber-Say syndrome's exact match is recorded as http://www.orpha.net/ORDO/Orphanet_1231^[24].
• Barber-Say syndrome's UMLS CUI is recorded as C1319466^[25].
• Barber-Say syndrome's ICD-10-CM is recorded as Q87.0^[26].
• Barber-Say syndrome's GARD rare disease ID is recorded as 819^[27].

Why It Matters

Barber-Say syndrome draws 154 Wikipedia views per month (developmental_defect_during_embryogenesis category, ranking #39 of 308).^[2] It has Wikipedia articles in 6 language editions, a strong signal of global cultural recognition.^[28] It is known by 9 alternative names across languages and contexts.^[29]