Abruzzo–Erickson syndrome
human disease
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Abruzzo–Erickson syndrome
Summary
Abruzzo–Erickson syndrome is a head and neck disease[1]. It has Wikipedia articles in 5 language editions, a strong signal of global cultural recognition.[2]
Key Facts
- Abruzzo–Erickson syndrome's instance of is recorded as head and neck disease[3].
- Abruzzo–Erickson syndrome's instance of is recorded as developmental defect during embryogenesis[4].
- Abruzzo–Erickson syndrome's instance of is recorded as rare disease[5].
- Abruzzo–Erickson syndrome's instance of is recorded as class of disease[6].
- Abruzzo–Erickson syndrome is a type of genetic deafness[7].
- Abruzzo–Erickson syndrome is a type of coloboma[8].
- Abruzzo–Erickson syndrome is a type of cleft lip and cleft palate[9].
- Abruzzo–Erickson syndrome is a type of multiple congenital anomalies/dysmorphic syndrome without intellectual disability[10].
- Abruzzo–Erickson syndrome is a type of orofacial clefting syndrome[11].
- Abruzzo–Erickson syndrome is a type of syndromic urogenital tract malformation[12].
- Abruzzo–Erickson syndrome is a type of syndrome[13].
- Abruzzo–Erickson syndrome is a type of X-linked disease[14].
- Abruzzo–Erickson syndrome is a type of disease[15].
- Abruzzo–Erickson syndrome's genetic association is recorded as TBX22[16].
- Abruzzo–Erickson syndrome's exact match is recorded as http://www.orpha.net/ORDO/Orphanet_921[17].
- Abruzzo–Erickson syndrome's exact match is recorded as http://purl.obolibrary.org/obo/DOID_0111826[18].
- Abruzzo–Erickson syndrome's exact match is recorded as http://identifiers.org/doid/DOID:0111826[19].
Why It Matters
Abruzzo–Erickson syndrome has Wikipedia articles in 5 language editions, a strong signal of global cultural recognition.[2] It is known by 10 alternative names across languages and contexts.[20]