diastematomyelia
rare congenital abnormality in which the spinal cord is split in half by fibrous or bony tissue. It may present as an isolated phenomenon or in association with spina bifida
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diastematomyelia
Summary
diastematomyelia is a developmental defect during embryogenesis[1]. diastematomyelia draws 155 Wikipedia views per month (developmental_defect_during_embryogenesis category, ranking #96 of 308).[2]
Key Facts
- diastematomyelia's instance of is recorded as developmental defect during embryogenesis[3].
- diastematomyelia's instance of is recorded as class of disease[4].
- diastematomyelia is a type of congenital vertebral anomaly[5].
- diastematomyelia is a type of malformation of the neurenteric canal, spinal cord and column[6].
- diastematomyelia's Commons category is recorded as Diastematomyelia[7].
- diastematomyelia's ICD-9-CM is recorded as 742.51[8].
- diastematomyelia's NCI Thesaurus ID is recorded as C98913[9].
- diastematomyelia's health specialty is recorded as medical genetics[10].
Why It Matters
diastematomyelia draws 155 Wikipedia views per month (developmental_defect_during_embryogenesis category, ranking #96 of 308).[2] diastematomyelia has Wikipedia articles in 5 language editions, a strong signal of global cultural recognition.[11] diastematomyelia is known by 9 alternative names across languages and contexts.[12]