DiseaseID 6734
野中肌病
disease
NCI2016_NICHD_1602D:A rare form of progressive muscle disease that is notable for cytoplasmic granules and vacuoles in the muscle with little inflammation, and is usually refractory to treatment. Usually symptoms begin a
Relationship Network
Interactive first-hop connections across herbs, ingredients, formulas, targets, diseases, symptoms, syndromes, evidence, and monographs.
Click a node to open it in a new tab
Disease: 1Experiment: 1Symptom: 5Target: 12Links: 18
Arranging relationship network...
Record Fields
Scalar fields from the final disease record.
- Disease Id
- 6734
- Core Entity Id
- 63429
- Source Entity Count
- 1
- Preferred Name
- Nonaka Myopathy
- Name Cn
- 野中肌病
- Name Pinyin
- Ye Zhong Ji Bing
- Name En
- Nonaka Myopathy
- Name Latin
- Bilingual Status
- complete
- Disease Type
- disease
- Umls Disease Type
- Disease or Syndrome
- Disgenet Type
- disease
- Mesh Class
- Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nervous System Diseases; Musculoskeletal DiseasesMusculoskeletal Diseases; Eye Diseases; Nervous System Diseases; Pathological Conditions, Signs and SymptomsNervous System Diseases; Musculoskeletal Diseases
- Do Class
- disease of anatomical entity
- Hpo Class
- Mesh Class Name
- Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Musculoskeletal Diseases; Nervous System DiseasesMusculoskeletal Diseases; Nervous System DiseasesPathological Conditions, Signs and Symptoms; Eye Diseases; Musculoskeletal Diseases; Nervous System Diseases
- Hpo Class Name
- Do Class Name
- disease of anatomical entity
- Disease Definition
- NCI2016_NICHD_1602D:A rare form of progressive muscle disease that is notable for cytoplasmic granules and vacuoles in the muscle with little inflammation, and is usually refractory to treatment. Usually symptoms begin after the age of fifty.|NCI2016_02D:An acquired or hereditary chronic inflammatory disorder of the muscles characterized by the morphologic finding of vacuoles and filamentous inclusions in the muscle tissues.|MSH2017_2016_08_12:Progressive myopathies characterized by the presence of inclusion bodies on muscle biopsy. Sporadic and hereditary forms have been described. The sporadic form is an acquired, adult-onset inflammatory vacuolar myopathy affecting proximal and distal muscles. Familial forms usually begin in childhood and lack inflammatory changes. Both forms feature intracytoplasmic and intranuclear inclusions in muscle tissue. (Adams et al., Principles of Neurology, 6th ed, pp1409-10)
- Version
- v1,v2
- Suppressed
- No
Names
Preferred names, aliases, and source labels retained in the final schema.
Name
Nonaka Myopathy
Role
preferred
Name
Inclusion Body Myopathy, Sporadic
Role
preferred
Name
Inclusion Body Myositis (Disorder)
Role
preferred
Name
INCLUSION BODY MYOPATHY 3, AUTOSOMAL DOMINANT
Role
preferred
Name
Distal Myopathy, Nonaka Type
Role
alias
Name
Inclusion Body Myositis
Role
alias
Name
Myopathy, Distal, With Rimmed Vacuoles
Role
alias
Name
Myopathy, Proximal, And Ophthalmoplegia
Role
alias
Name
Myositis, Inclusion Body
Role
alias
Cross References
Trusted external identifiers retained for this final record.
Herb
HBDIS005132HBDIS011430HBDIS016994HBDIS017009
Me Sh
D018979
Omim
147421605637605820617158
Umls
C0238190C0751713
Icd10
G72.41
Sym Map
SMDE01507SMDE09813SMDE09814
Do Class
DOID:7
Dis Ge Net
C0238190C0751713C1853926C1854106
Umls Sty
T047
Me Sh Class
C05C10C11C16C23
Tcmbank Disease
107516557246826158
Itcmdb Generated
ITX-DISEASE-7C8AEF038505
Attributes
Merged source attributes and domain-specific metadata.
Version
v1,v2v2
Suppress
0
Do Class Name
disease of anatomical entity
Disease Type
disease
Do Disease Class
disease of anatomical entity
Umls Disease Type
Disease or Syndrome
Disease Definition
NCI2016_NICHD_1602D:A rare form of progressive muscle disease that is notable for cytoplasmic granules and vacuoles in the muscle with little inflammation, and is usually refractory to treatment. Usually symptoms begin after the age of fifty.|NCI2016_02D:An acquired or hereditary chronic inflammatory disorder of the muscles characterized by the morphologic finding of vacuoles and filamentous inclusions in the muscle tissues.|MSH2017_2016_08_12:Progressive myopathies characterized by the presence of inclusion bodies on muscle biopsy. Sporadic and hereditary forms have been described. The sporadic form is an acquired, adult-onset inflammatory vacuolar myopathy affecting proximal and distal muscles. Familial forms usually begin in childhood and lack inflammatory changes. Both forms feature intracytoplasmic and intranuclear inclusions in muscle tissue. (Adams et al., Principles of Neurology, 6th ed, pp1409-10)
Me Sh Disease Class
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nervous System Diseases; Musculoskeletal DiseasesMusculoskeletal Diseases; Eye Diseases; Nervous System Diseases; Pathological Conditions, Signs and SymptomsNervous System Diseases; Musculoskeletal Diseases
Dis Ge Net Disease Type
disease
Disease Class Name Me Sh
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Musculoskeletal Diseases; Nervous System DiseasesMusculoskeletal Diseases; Nervous System DiseasesPathological Conditions, Signs and Symptoms; Eye Diseases; Musculoskeletal Diseases; Nervous System Diseases
Umls Semantic Type Name
Disease or Syndrome