Barber-Say syndrome
rare genetic disorder
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Barber-Say syndrome
Summary
Barber-Say syndrome is a developmental defect during embryogenesis[1]. It draws 67 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 is a type of ectodermal dysplasia[6].
- Barber-Say syndrome is a type of syndrome[7].
- Barber-Say syndrome is a type of hypertrichosis of eyelid[8].
- Barber-Say syndrome is a type of secondary ectropion[9].
- Barber-Say syndrome is a type of microblepharon-ablephara syndrome[10].
- Barber-Say syndrome is a type of congenital entropion[11].
- Barber-Say syndrome is a type of syndromic developmental defect of the eye[12].
- Barber-Say syndrome is a type of multiple congenital anomalies/dysmorphic syndrome without intellectual disability[13].
- Barber-Say syndrome's genetic association is recorded as TWIST2[14].
- Barber-Say syndrome's exact match is recorded as http://purl.obolibrary.org/obo/DOID_0060549[15].
- Barber-Say syndrome's exact match is recorded as http://identifiers.org/doid/DOID:0060549[16].
- Barber-Say syndrome's exact match is recorded as http://www.orpha.net/ORDO/Orphanet_1231[17].
- Barber-Say syndrome's on focus list of Wikimedia project is recorded as WikiProject Medicine[18].
Why It Matters
Barber-Say syndrome draws 67 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.[19] It is known by 9 alternative names across languages and contexts.[20]