Spina bifida
MONDO:0008449A congenital neural tube defect in which vertebrae are not fully formed. It results in the protrusion of the spinal cord through the opening of the vertebrae.
Also known as: rachischisis, spina bifida, spina bifida (disease), spinal meningocele, spinal myelocele, spinal myelomeningocele, NTD, neural tube defects, susceptibility to
59 clinical trials for this condition and its sub-types, 44 tagged with Spina bifida itself.
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Sub-types of Spina bifida
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Isolated spina bifida 1 trial · 28 incl. sub-types
4 sub-types
- Spina bifida cystica 1 trial · 26 incl. sub-types Sub-types →
- Spina bifida aperta 1 trial · 4 incl. sub-types Sub-types →
- Neural tube defects, X-linked 0 trials
- Neural tube defects, folate-sensitive 0 trials
-
Spina bifida occulta 2 trials
2 sub-types
- Dysraphic spinal cord lipoma 0 trials Sub-types →
- Dysraphism with stalk 0 trials Sub-types →
Most studied deeper sub-types
Myelomeningocele
(25)
Myeloschisis
(3)
Chiari malformation type II
(2)
Cervical spina bifida aperta
(0)
Cervical spina bifida cystica
(0)
Cervicothoracic spina bifida aperta
(0)
Cervicothoracic spina bifida cystica
(0)
Chaotic conus spinal cord lipoma
(0)
Conus spinal cord lipoma
(0)
Dorsal spinal cord lipoma
(0)
Extramedullary conus spinal cord lipoma
(0)
Fibroneural non-saccular limited dorsal myeloschisis
(0)
Hemi-myelomeningocele
(0)
Hemi-myeloschisis
(0)
Isolated filum lipoma
(0)
Isolated transitional filum lipoma
(0)
Limited dorsal myeloschisis
(0)
Lipomatous non-saccular limited dorsal myeloschisis
(0)
Lumbosacral spina bifida aperta
(0)
Lumbosacral spina bifida cystica
(0)