Relationship Network
Interactive first-hop connections across herbs, ingredients, formulas, targets, diseases, symptoms, syndromes, evidence, and monographs.
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Disease: 1Symptom: 5Target: 18Links: 29
Arranging relationship network...
Record Fields
Scalar fields from the final disease record.
- Disease Id
- 12186
- Core Entity Id
- 69669
- Source Entity Count
- 1
- Preferred Name
- Muscular Dystrophy Congenital, Merosin Negative
- Name Cn
- 先天性肌营养不良，分区蛋白阴性型
- Name Pinyin
- Xian Tian Xing Ji Ying Yang Bu Liang ， Fen Qu Dan Bai Yin Xing Xing
- Name En
- Muscular Dystrophy Congenital, Merosin Negative
- 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 Diseases
- Do Class
- disease of anatomical entity; genetic disease
- Hpo Class
- Mesh Class Name
- Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Musculoskeletal Diseases; Nervous System Diseases
- Hpo Class Name
- Do Class Name
- genetic disease; disease of anatomical entity
- Disease Definition
- Version
- v1
- Suppressed
- No
Names
Preferred names, aliases, and source labels retained in the final schema.
Name
Muscular Dystrophy Congenital, Merosin Negative
Role
preferred
Name
Muscular Dystrophy, Congenital, Due To Partial Lama2 Deficiency
Role
preferred
Name
Muscular Dystrophy, Congenital Merosin-Deficient, 1A
Role
preferred
Name
Congenital Merosin-Deficient Muscular Dystrophy 1A
Role
alias
Name
Muscular Dystrophy, Congenital Merosin-Deficient
Role
alias
Cross References
Trusted external identifiers retained for this final record.
Herb
HBDIS012910HBDIS015977
Omim
607855
Umls
C1842898
Sym Map
SMDE01639SMDE11174
Do Class
DOID:630DOID:7
Dis Ge Net
C1263858C1842898
Umls Sty
T047
Me Sh Class
C05C10C16
Etcm Disease
Muscular Dystrophy, Congenital Merosin-Deficient, 1a
Tcmbank Disease
199544482
Itcmdb Generated
ITX-DISEASE-107260B73E6A
Attributes
Merged source attributes and domain-specific metadata.
Version
v1v2
Suppress
0
Page Title
Disease Muscular Dystrophy, Congenital Merosin-Deficient, 1a Details page
Do Class Name
genetic disease; disease of anatomical entity
Disease Type
disease
Do Disease Class
disease of anatomical entity; genetic disease
Umls Disease Type
Disease or Syndrome
Basic Information
Disease Name
Muscular Dystrophy, Congenital Merosin-Deficient, 1a
Global Category
Genetic diseases
Anatomical Category
Cardiovascular diseases;Muscle diseases;Neuronal diseases
Me Sh Disease Class
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nervous 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 Diseases
Umls Semantic Type Name
Disease or Syndrome