DiseaseID 5489
隐性脊柱裂
disease
NCI2016_02D:The mildest form of spina bifida, characterized by any of several neural tube defects which may go undetected until an x-ray is performed. Treatment is symptomatic.|MSH2017_2016_08_12:A common congenital midl
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Disease: 1Symptom: 4Target: 12Links: 16
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Record Fields
Scalar fields from the final disease record.
- Disease Id
- 5489
- Core Entity Id
- 61998
- Source Entity Count
- 1
- Preferred Name
- Spina Bifida Occulta
- Name Cn
- 隐性脊柱裂
- Name Pinyin
- Yin Xing Ji Zhu Lie
- Name En
- Spina Bifida Occulta
- Name Latin
- Bilingual Status
- complete
- Disease Type
- disease
- Umls Disease Type
- Congenital Abnormality
- Disgenet Type
- disease
- Mesh Class
- Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nervous System Diseases
- Do Class
- physical disorder
- Hpo Class
- Abnormality of the nervous system
- Mesh Class Name
- Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nervous System Diseases
- Hpo Class Name
- Abnormality of the nervous system
- Do Class Name
- physical disorder
- Disease Definition
- NCI2016_02D:The mildest form of spina bifida, characterized by any of several neural tube defects which may go undetected until an x-ray is performed. Treatment is symptomatic.|MSH2017_2016_08_12:A common congenital midline defect of fusion of the vertebral arch without protrusion of the spinal cord or meninges. The lesion is also covered by skin. L5 and S1 are the most common vertebrae involved. The condition may be associated with an overlying area of hyperpigmented skin, a dermal sinus, or an abnormal patch of hair. The majority of individuals with this malformation are asymptomatic although there is an increased incidence of tethered cord syndrome and lumbar SPONDYLOSIS. (From Joynt, Clinical Neurology, 1992, Ch55, p34)|HPO2016_07_04:The closed form of spina bifida with incomplete closure of a vertebral body with intact overlying skin. [HPO:probinson]
- Version
- v2
- Suppressed
- No
Names
Preferred names, aliases, and source labels retained in the final schema.
Name
Spina Bifida Occulta
Role
preferred
Cross References
Trusted external identifiers retained for this final record.
Hpo
HP:0003298
Herb
HBDIS003223
Me Sh
D016136
Umls
C0080174
Icd10
Q76.0
Sym Map
SMDE13332
Do Class
DOID:0080015
Dis Ge Net
C0080174
Umls Sty
T019
Hpo Class
HP:0000707
Me Sh Class
C10C16
Tcmbank Disease
2728
Attributes
Merged source attributes and domain-specific metadata.
Version
v2
Suppress
0
Do Class Name
physical disorder
Disease Type
disease
Hpo Class Name
Abnormality of the nervous system
Do Disease Class
physical disorder
Hpo Disease Class
Abnormality of the nervous system
Umls Disease Type
Congenital Abnormality
Disease Definition
NCI2016_02D:The mildest form of spina bifida, characterized by any of several neural tube defects which may go undetected until an x-ray is performed. Treatment is symptomatic.|MSH2017_2016_08_12:A common congenital midline defect of fusion of the vertebral arch without protrusion of the spinal cord or meninges. The lesion is also covered by skin. L5 and S1 are the most common vertebrae involved. The condition may be associated with an overlying area of hyperpigmented skin, a dermal sinus, or an abnormal patch of hair. The majority of individuals with this malformation are asymptomatic although there is an increased incidence of tethered cord syndrome and lumbar SPONDYLOSIS. (From Joynt, Clinical Neurology, 1992, Ch55, p34)|HPO2016_07_04:The closed form of spina bifida with incomplete closure of a vertebral body with intact overlying skin. [HPO:probinson]
Me Sh Disease Class
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nervous System Diseases
Dis Ge Net Disease Type
disease
Disease Class Name Me Sh
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nervous System Diseases
Umls Semantic Type Name
Congenital Abnormality