Relationship Network
Interactive first-hop connections across herbs, ingredients, formulas, targets, diseases, symptoms, syndromes, evidence, and monographs.
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Disease: 1Formula: 7Herb: 12Target: 17Links: 43
Arranging relationship network...
Record Fields
Scalar fields from the final disease record.
- Disease Id
- 2552
- Core Entity Id
- 2888
- Source Entity Count
- 1
- Preferred Name
- Emery-Dreifuss Muscular Dystrophy 7, Autosomal Dominant
- Name Cn
- Emery-Dreifuss肌营养不良7型，常染色体显性遗传
- Name Pinyin
- Emery-dreifuss Ji Ying Yang Bu Liang 7 Xing ， Chang Ran Se Ti Xian Xing Yi Chuan
- Name En
- Emery-Dreifuss Muscular Dystrophy 7, Autosomal Dominant
- Name Latin
- Bilingual Status
- complete
- Disease Type
- Umls Disease Type
- Disease or Syndrome
- Disgenet Type
- disease
- Mesh Class
- Do Class
- disease of anatomical entity; genetic disease
- Hpo Class
- Mesh Class Name
- Hpo Class Name
- Do Class Name
- Disease Definition
- Version
- v1
- Suppressed
- No
Names
Preferred names, aliases, and source labels retained in the final schema.
Name
Emery-Dreifuss Muscular Dystrophy 7, Autosomal Dominant
Role
preferred
Name
Autosomal Dominant Emery-Dreifuss Muscular Dystrophy 7
Role
alias
Name
EDMD7
Role
alias
Cross References
Trusted external identifiers retained for this final record.
Herb
HBDIS029387
Omim
614302
Umls
C3553060
Sym Map
SMDE04164
Do Class
DOID:630DOID:7
Dis Ge Net
C3553060
Umls Sty
T047
Etcm Disease
Emery-Dreifuss Muscular Dystrophy 7, Autosomal Dominant
Itcmdb Generated
ITX-DISEASE-CD8E2F0A4D91
Attributes
Merged source attributes and domain-specific metadata.
Version
v1
Suppress
0
Page Title
Disease Emery-Dreifuss Muscular Dystrophy 7, Autosomal Dominant Details page
Do Disease Class
disease of anatomical entity; genetic disease
Umls Disease Type
Disease or Syndrome
Basic Information
Disease Name
Emery-Dreifuss Muscular Dystrophy 7, Autosomal Dominant
Global Category
Genetic diseases;Rare diseases
Anatomical Category
Bone diseases;Cardiovascular diseases;Muscle diseases;Neuronal diseases
Dis Ge Net Disease Type
disease