DiseaseID 2322
神经源性先天性多发性关节弯曲（疾病）
disease
SNOMEDCT_US_2016_09_01:A form of arthrogryposis multiplex congenital characterized by congenital immobility of the limbs with fixation of multiple joints and muscle wasting. This condition is caused by neurogenic muscula
Relationship Network
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Disease: 1Symptom: 1Target: 6Links: 7
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Record Fields
Scalar fields from the final disease record.
- Disease Id
- 2322
- Core Entity Id
- 2615
- Source Entity Count
- 1
- Preferred Name
- Arthrogryposis Multiplex Congenita, Neurogenic Type (Disorder)
- Name Cn
- 神经源性先天性多发性关节弯曲（疾病）
- Name Pinyin
- Shen Jing Yuan Xing Xian Tian Xing Duo Fa Xing Guan Jie Wan Qu （ Ji Bing ）
- Name En
- Arthrogryposis Multiplex Congenita, Neurogenic Type (Disorder)
- Name Latin
- Bilingual Status
- complete
- Disease Type
- Umls Disease Type
- Disease or Syndrome
- Disgenet Type
- disease
- Mesh Class
- Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Musculoskeletal Diseases
- Do Class
- disease of anatomical entity; genetic disease
- Hpo Class
- Mesh Class Name
- Hpo Class Name
- Do Class Name
- Disease Definition
- SNOMEDCT_US_2016_09_01:A form of arthrogryposis multiplex congenital characterized by congenital immobility of the limbs with fixation of multiple joints and muscle wasting. This condition is caused by neurogenic muscular atrophy.|SNOMEDCT_US_2016_09_01:A form of arthrogryposis multiplex congenital characterised by congenital immobility of the limbs with fixation of multiple joints and muscle wasting. This condition is caused by neurogenic muscular atrophy.
- Version
- v2
- Suppressed
- No
Names
Preferred names, aliases, and source labels retained in the final schema.
Name
Arthrogryposis Multiplex Congenita, Neurogenic Type (Disorder)
Role
preferred
Name
Amc, Neurogenic Type
Role
alias
Name
Arthrogryposis Multiplex Congenita Neurogenic Type
Role
alias
Name
Arthrogryposis Multiplex Congenita, Neurogenic Type
Role
alias
Name
Neurogenic Arthrogryposis Multiplex Congenita
Role
alias
Cross References
Trusted external identifiers retained for this final record.
Herb
HBDIS028984
Umls
C1859721
Sym Map
SMDE06055
Do Class
DOID:630DOID:7
Dis Ge Net
C1859721
Umls Sty
T047
Me Sh Class
C05C16
Attributes
Merged source attributes and domain-specific metadata.
Version
v2
Suppress
0
Do Disease Class
disease of anatomical entity; genetic disease
Umls Disease Type
Disease or Syndrome
Disease Definition
SNOMEDCT_US_2016_09_01:A form of arthrogryposis multiplex congenital characterized by congenital immobility of the limbs with fixation of multiple joints and muscle wasting. This condition is caused by neurogenic muscular atrophy.|SNOMEDCT_US_2016_09_01:A form of arthrogryposis multiplex congenital characterised by congenital immobility of the limbs with fixation of multiple joints and muscle wasting. This condition is caused by neurogenic muscular atrophy.
Me Sh Disease Class
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Musculoskeletal Diseases
Dis Ge Net Disease Type
disease