Relationship Network
Interactive first-hop connections across herbs, ingredients, formulas, targets, diseases, symptoms, syndromes, evidence, and monographs.
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Disease: 1Target: 1Links: 1
Arranging relationship network...
Record Fields
Scalar fields from the final disease record.
- Disease Id
- 14215
- Core Entity Id
- 71968
- Source Entity Count
- 1
- Preferred Name
- Spondyloepimetaphyseal Dysplasia, Matrilin-3 Related
- Name Cn
- 脊柱骨骺干骺端发育不良，Matrilin-3相关
- Name Pinyin
- Ji Zhu Gu Hou Gan Hou Duan Fa Yu Bu Liang ，matrilin-3 Xiang Guan
- Name En
- Spondyloepimetaphyseal Dysplasia, Matrilin-3 Related
- 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; Musculoskeletal Diseases
- Do Class
- Hpo Class
- Mesh Class Name
- Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Musculoskeletal Diseases
- 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
Spondyloepimetaphyseal Dysplasia, Matrilin-3 Related
Role
preferred
Name
SEMD, MATN3-RELATED
Role
alias
Cross References
Trusted external identifiers retained for this final record.
Herb
HBDIS015577
Omim
608728
Umls
C1837481
Sym Map
SMDE03005
Dis Ge Net
C1837481
Umls Sty
T047
Me Sh Class
C05C16
Tcmbank Disease
22209
Attributes
Merged source attributes and domain-specific metadata.
Version
v1
Suppress
0
Disease Type
disease
Umls Disease Type
Disease or Syndrome
Me Sh Disease Class
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Musculoskeletal Diseases
Dis Ge Net Disease Type
disease
Disease Class Name Me Sh
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Musculoskeletal Diseases
Umls Semantic Type Name
Disease or Syndrome