lateral meningocele syndrome
human disease
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lateral meningocele syndrome
Summary
lateral meningocele syndrome is a developmental defect during embryogenesis[1].
Key Facts
- lateral meningocele syndrome's instance of is recorded as developmental defect during embryogenesis[2].
- lateral meningocele syndrome's instance of is recorded as class of disease[3].
- lateral meningocele syndrome is a type of malformation of the neurenteric canal, spinal cord and column[4].
- lateral meningocele syndrome is a type of syndrome[5].
- lateral meningocele syndrome is a type of autosomal dominant disease[6].
- lateral meningocele syndrome's genetic association is recorded as NOTCH3[7].
- lateral meningocele syndrome's exact match is recorded as http://www.orpha.net/ORDO/Orphanet_2789[8].
- lateral meningocele syndrome's exact match is recorded as http://purl.obolibrary.org/obo/DOID_0111343[9].
- lateral meningocele syndrome's exact match is recorded as http://identifiers.org/doid/DOID:0111343[10].