Donnai-Barrow syndrome
human disease
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Donnai-Barrow syndrome
Summary
Donnai-Barrow syndrome is a developmental defect during embryogenesis[1]. It has Wikipedia articles in 7 language editions, a strong signal of global cultural recognition.[2]
Key Facts
- Donnai-Barrow syndrome's instance of is recorded as developmental defect during embryogenesis[3].
- Donnai-Barrow syndrome's instance of is recorded as rare disease[4].
- Donnai-Barrow syndrome's instance of is recorded as class of disease[5].
- Dian Donnai is named after Donnai-Barrow syndrome[6].
- Donnai-Barrow syndrome is a type of autosomal recessive disease[7].
- Donnai-Barrow syndrome is a type of rare genetic developmental defect during embryogenesis[8].
- Donnai-Barrow syndrome is a type of multiple congenital anomalies/dysmorphic syndrome-variable intellectual disability syndrome[9].
- Donnai-Barrow syndrome is a type of syndromic diaphragmatic or abdominal wall malformation[10].
- Donnai-Barrow syndrome is a type of syndromic diaphragmatic or thoracic malformation[11].
- Donnai-Barrow syndrome is a type of syndrome[12].
- Donnai-Barrow syndrome's ICD-9-CM is recorded as 759.89[13].
- Donnai-Barrow syndrome's health specialty is recorded as medical genetics[14].
- Donnai-Barrow syndrome's genetic association is recorded as LRP2[15].
- Donnai-Barrow syndrome's exact match is recorded as http://purl.obolibrary.org/obo/DOID_0090144[16].
- Donnai-Barrow syndrome's exact match is recorded as http://identifiers.org/doid/DOID:0090144[17].
- Donnai-Barrow syndrome's exact match is recorded as http://www.orpha.net/ORDO/Orphanet_2143[18].
- Donnai-Barrow syndrome's on focus list of Wikimedia project is recorded as WikiProject Medicine[19].
Why It Matters
Donnai-Barrow syndrome has Wikipedia articles in 7 language editions, a strong signal of global cultural recognition.[2] It is known by 14 alternative names across languages and contexts.[20]