myelomeningocele
spina bifida characterized by protrusion of the spinal cord through an opening, covered by meningeal membranes
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myelomeningocele
Summary
myelomeningocele is a developmental defect during embryogenesis[1].
Key Facts
- myelomeningocele's instance of is recorded as developmental defect during embryogenesis[2].
- myelomeningocele's instance of is recorded as designated intractable/rare disease[3].
- myelomeningocele's instance of is recorded as class of disease[4].
- myelomeningocele is a type of meningocele[5].
- myelomeningocele is a type of spina bifida[6].
- myelomeningocele is a type of spinal cord disease[7].
- myelomeningocele's Commons category is recorded as Spina bifida[8].
- myelomeningocele's anatomical location is recorded as spinal cord[9].
- myelomeningocele's external data available at URL is recorded as http://www.nanbyou.or.jp/entry/4633[10].
- myelomeningocele's NCI Thesaurus ID is recorded as C101201[11].
- myelomeningocele's NCI Thesaurus ID is recorded as C98874[12].
- myelomeningocele's health specialty is recorded as medical genetics[13].
- myelomeningocele's exact match is recorded as http://purl.obolibrary.org/obo/DOID_0060326[14].
- myelomeningocele's exact match is recorded as http://identifiers.org/doid/DOID:0060326[15].
- myelomeningocele's exact match is recorded as http://purl.obolibrary.org/obo/HP_0002475[16].
- myelomeningocele's exact match is recorded as http://www.orpha.net/ORDO/Orphanet_93969[17].
- myelomeningocele's on focus list of Wikimedia project is recorded as WikiProject Medicine[18].