DiseaseID 4843
热带痉挛性截瘫
disease
SNOMEDCT_US_2016_09_01:A progressive chronic inflammatory disease of the central nervous system with the etiologic agent Human T cell lymphotropic virus type I (HTLV-I), the disease is characterized by unremitting myelop
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Disease: 1Symptom: 2Target: 12Links: 14
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Record Fields
Scalar fields from the final disease record.
- Disease Id
- 4843
- Core Entity Id
- 61256
- Source Entity Count
- 1
- Preferred Name
- Tropical Spastic Paraparesis
- Name Cn
- 热带痉挛性截瘫
- Name Pinyin
- Re Dai Jing Luan Xing Jie Tan
- Name En
- Tropical Spastic Paraparesis
- Name Latin
- Bilingual Status
- complete
- Disease Type
- disease
- Umls Disease Type
- Disease or Syndrome
- Disgenet Type
- disease
- Mesh Class
- Infections; Nervous System Diseases
- Do Class
- disease of anatomical entity; disease by infectious agent
- Hpo Class
- Mesh Class Name
- Infections; Nervous System Diseases
- Hpo Class Name
- Do Class Name
- disease of anatomical entity; disease by infectious agent
- Disease Definition
- SNOMEDCT_US_2016_09_01:A progressive chronic inflammatory disease of the central nervous system with the etiologic agent Human T cell lymphotropic virus type I (HTLV-I), the disease is characterized by unremitting myelopathic symptoms such as spastic paraparesis, bowel and/or bladder dysfunction and sensory changes of the lower limbs.|SNOMEDCT_US_2016_09_01:A progressive chronic inflammatory disease of the central nervous system with the aetiologic agent Human T cell lymphotropic virus type I (HTLV-I), the disease is characterised by unremitting myelopathic symptoms such as spastic paraparesis, bowel and/or bladder dysfunction and sensory changes of the lower limbs.|MSH2017_2016_08_12:A subacute paralytic myeloneuropathy occurring endemically in tropical areas such as the Caribbean, Colombia, India, and Africa, as well as in the southwestern region of Japan; associated with infection by HUMAN T-CELL LEUKEMIA VIRUS I. Clinical manifestations include a slowly progressive spastic weakness of the legs, increased reflexes, Babinski signs, incontinence, and loss of vibratory and position sensation. On pathologic examination inflammatory, demyelination, and necrotic lesions may be found in the spinal cord. (Adams et al., Principles of Neurology, 6th ed, p1239)|CHV2011_02:an incurable viral infection of the spinal cord that causes weakness in the legs|CHV2011_02:an incurable viral infection of the spinal cord that causes weakness in the legs|CHV2011_02:an incurable viral infection of the spinal cord that causes weakness in the legs|CHV2011_02:an incurable viral infection of the spinal cord that causes weakness in the legs|CHV2011_02:an incurable viral infection of the spinal cord that causes weakness in the legs|CHV2011_02:an incurable viral infection of the spinal cord that causes weakness in the legs
- Version
- v2
- Suppressed
- No
Names
Preferred names, aliases, and source labels retained in the final schema.
Name
Tropical Spastic Paraparesis
Role
preferred
Name
Myelopathy, Htlv-1-Associated
Role
alias
Name
Paraparesis, Tropical Spastic
Role
alias
Name
Tropical Spastic Paraplegia
Role
alias
Cross References
Trusted external identifiers retained for this final record.
Herb
HBDIS002301
Me Sh
D015493
Omim
159580
Umls
C0030481
Icd10
G04.1
Sym Map
SMDE14019
Do Class
DOID:0050117DOID:7
Dis Ge Net
C0030481
Umls Sty
T047
Me Sh Class
C01C10
Tcmbank Disease
16994
Attributes
Merged source attributes and domain-specific metadata.
Version
v2
Suppress
0
Do Class Name
disease of anatomical entity; disease by infectious agent
Disease Type
disease
Do Disease Class
disease of anatomical entity; disease by infectious agent
Umls Disease Type
Disease or Syndrome
Disease Definition
SNOMEDCT_US_2016_09_01:A progressive chronic inflammatory disease of the central nervous system with the etiologic agent Human T cell lymphotropic virus type I (HTLV-I), the disease is characterized by unremitting myelopathic symptoms such as spastic paraparesis, bowel and/or bladder dysfunction and sensory changes of the lower limbs.|SNOMEDCT_US_2016_09_01:A progressive chronic inflammatory disease of the central nervous system with the aetiologic agent Human T cell lymphotropic virus type I (HTLV-I), the disease is characterised by unremitting myelopathic symptoms such as spastic paraparesis, bowel and/or bladder dysfunction and sensory changes of the lower limbs.|MSH2017_2016_08_12:A subacute paralytic myeloneuropathy occurring endemically in tropical areas such as the Caribbean, Colombia, India, and Africa, as well as in the southwestern region of Japan; associated with infection by HUMAN T-CELL LEUKEMIA VIRUS I. Clinical manifestations include a slowly progressive spastic weakness of the legs, increased reflexes, Babinski signs, incontinence, and loss of vibratory and position sensation. On pathologic examination inflammatory, demyelination, and necrotic lesions may be found in the spinal cord. (Adams et al., Principles of Neurology, 6th ed, p1239)|CHV2011_02:an incurable viral infection of the spinal cord that causes weakness in the legs|CHV2011_02:an incurable viral infection of the spinal cord that causes weakness in the legs|CHV2011_02:an incurable viral infection of the spinal cord that causes weakness in the legs|CHV2011_02:an incurable viral infection of the spinal cord that causes weakness in the legs|CHV2011_02:an incurable viral infection of the spinal cord that causes weakness in the legs|CHV2011_02:an incurable viral infection of the spinal cord that causes weakness in the legs
Me Sh Disease Class
Infections; Nervous System Diseases
Dis Ge Net Disease Type
disease
Disease Class Name Me Sh
Infections; Nervous System Diseases
Umls Semantic Type Name
Disease or Syndrome