Descriptor English: | Spinal Dysraphism | ||||||
Descriptor Spanish: |
Disrafia Espinal
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Descriptor Portuguese: | Disrafismo Espinal | ||||||
Descriptor French: | Dysraphie spinale | ||||||
Entry term(s): |
Bifida, Spina Cleft Spine Cleft Spines Dysraphia, Spinal Dysraphicus, Status Dysraphism, Spinal Dysraphisms, Spinal Open Spine Open Spines Rachischises Rachischisis Schistorrhachis Spina Bifida Spina Bifidas Spinal Dysraphia Spinal Dysraphias Spinal Dysraphisms Spine, Cleft Spine, Open Status Dysraphicus |
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Tree number(s): |
C10.500.680.800 C16.131.666.680.800 |
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RDF Unique Identifier: | https://id.nlm.nih.gov/mesh/D016135 | ||||||
Scope note: | Congenital defects of closure of one or more vertebral arches, which may be associated with malformations of the spinal cord, nerve roots, congenital fibrous bands, lipomas, and congenital cysts. These malformations range from mild (e.g., SPINA BIFIDA OCCULTA) to severe, including rachischisis where there is complete failure of neural tube and spinal cord fusion, resulting in exposure of the spinal cord at the surface. Spinal dysraphism includes all forms of spina bifida. The open form is called SPINA BIFIDA CYSTICA and the closed form is SPINA BIFIDA OCCULTA. (From Joynt, Clinical Neurology, 1992, Ch55, p34) |
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Annotation: | general or unspecified; prefer specifics |
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Allowable Qualifiers: |
BL blood CF cerebrospinal fluid CI chemically induced CL classification CO complications DG diagnostic imaging DH diet therapy DI diagnosis DT drug therapy EC economics EH ethnology EM embryology EN enzymology EP epidemiology ET etiology GE genetics HI history IM immunology ME metabolism MI microbiology MO mortality NU nursing PA pathology PC prevention & control PP physiopathology PS parasitology PX psychology RH rehabilitation RT radiotherapy SU surgery TH therapy UR urine VE veterinary VI virology |
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Public MeSH Note: | 1991; see STATUS DYSRAPHICUS 1964-90 ; for SPINA BIFIDA see SPINA BIFIDA OCCULTA 1978-1990, see SPINAL DYSRAPHISM 1966-1977 |
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History Note: | 1991(1964); for SPINA BIFIDA use SPINA BIFIDA OCCULTA 1978-1990, use SPINAL DYSRAPHISM 1966-1970 |
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DeCS ID: | 29127 | ||||||
Unique ID: | D016135 | ||||||
NLM Classification: | WE 730 | ||||||
Documents indexed in the Virtual Health Library (VHL): | Click here to access the VHL documents | ||||||
Date Established: | 1991/01/01 | ||||||
Date of Entry: | 1990/07/27 | ||||||
Revision Date: | 2018/07/02 |
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Spinal Dysraphism
- Preferred
Status Dysraphicus
- Broader
Rachischisis
- Narrower
Concept UI |
M0024641 |
Scope note | Congenital defects of closure of one or more vertebral arches, which may be associated with malformations of the spinal cord, nerve roots, congenital fibrous bands, lipomas, and congenital cysts. These malformations range from mild (e.g., SPINA BIFIDA OCCULTA) to severe, including rachischisis where there is complete failure of neural tube and spinal cord fusion, resulting in exposure of the spinal cord at the surface. Spinal dysraphism includes all forms of spina bifida. The open form is called SPINA BIFIDA CYSTICA and the closed form is SPINA BIFIDA OCCULTA. (From Joynt, Clinical Neurology, 1992, Ch55, p34) |
Preferred term | Spinal Dysraphism |
Entry term(s) |
Bifida, Spina Cleft Spine Cleft Spines Dysraphia, Spinal Dysraphism, Spinal Dysraphisms, Spinal Open Spine Open Spines Schistorrhachis Spina Bifida Spina Bifidas Spinal Dysraphia Spinal Dysraphias Spinal Dysraphisms Spine, Cleft Spine, Open |
Concept UI |
M0024640 |
Preferred term | Status Dysraphicus |
Entry term(s) |
Dysraphicus, Status |
Concept UI |
M0337008 |
Preferred term | Rachischisis |
Entry term(s) |
Rachischises |
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