Marden–Walker syndrome
medical condition
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Marden–Walker syndrome
Summary
Marden–Walker syndrome is a head and neck disease[1]. It draws 11 Wikipedia views per month (head_and_neck_disease category, ranking #52 of 92).[2]
Key Facts
- Marden–Walker syndrome's instance of is recorded as head and neck disease[3].
- Marden–Walker syndrome's instance of is recorded as developmental defect during embryogenesis[4].
- Marden–Walker syndrome's instance of is recorded as rare disease[5].
- Marden–Walker syndrome's instance of is recorded as class of disease[6].
- Marden–Walker syndrome is a type of neurogenic arthrogryposis multiplex congenita[7].
- Marden–Walker syndrome is a type of arthrogryposis multiplex congenita[8].
- Marden–Walker syndrome is a type of multiple congenital anomalies/dysmorphic syndrome-intellectual disability[9].
- Marden–Walker syndrome is a type of syndrome or malformation associated with head and neck malformations[10].
- Marden–Walker syndrome is a type of genetic syndromic intellectual disability[11].
- Marden–Walker syndrome is a type of rare genetic bone disease[12].
- Marden–Walker syndrome's ICD-9-CM is recorded as 759.89[13].
- Marden–Walker syndrome's genetic association is recorded as PIEZO2[14].
- Marden–Walker syndrome's exact match is recorded as http://www.orpha.net/ORDO/Orphanet_2461[15].
Why It Matters
Marden–Walker syndrome draws 11 Wikipedia views per month (head_and_neck_disease category, ranking #52 of 92).[2] It has Wikipedia articles in 6 language editions, a strong signal of global cultural recognition.[16] It is known by 4 alternative names across languages and contexts.[17]