branchiooculofacial syndrome
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branchiooculofacial syndrome
Summary
branchiooculofacial syndrome is a malformation syndrome[1]. It has Wikipedia articles in 5 language editions, a strong signal of global cultural recognition.[2]
Key Facts
- branchiooculofacial syndrome's instance of is recorded as malformation syndrome[3].
- branchiooculofacial syndrome's instance of is recorded as head and neck disease[4].
- branchiooculofacial syndrome's instance of is recorded as developmental defect during embryogenesis[5].
- branchiooculofacial syndrome's instance of is recorded as rare disease[6].
- branchiooculofacial syndrome's instance of is recorded as class of disease[7].
- branchiooculofacial syndrome is a type of autosomal dominant disease[8].
- branchiooculofacial syndrome is a type of multiple congenital anomalies/dysmorphic syndrome without intellectual disability[9].
- branchiooculofacial syndrome is a type of orofacial clefting syndrome[10].
- branchiooculofacial syndrome is a type of rare genetic bone disease[11].
- branchiooculofacial syndrome is a type of syndrome[12].
- branchiooculofacial syndrome's ICD-9-CM is recorded as 759.89[13].
- branchiooculofacial syndrome's genetic association is recorded as TFAP2A[14].
- branchiooculofacial syndrome's exact match is recorded as http://purl.obolibrary.org/obo/DOID_0050691[15].
- branchiooculofacial syndrome's exact match is recorded as http://identifiers.org/doid/DOID:0050691[16].
- branchiooculofacial syndrome's exact match is recorded as http://www.orpha.net/ORDO/Orphanet_1297[17].
- branchiooculofacial syndrome's on focus list of Wikimedia project is recorded as WikiProject Medicine[18].
Why It Matters
branchiooculofacial syndrome has Wikipedia articles in 5 language editions, a strong signal of global cultural recognition.[2] It is known by 12 alternative names across languages and contexts.[19]