DiseaseID 14817

X连锁脊椎干骺端发育不良

disease

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Relationship Network

Interactive first-hop connections across herbs, ingredients, formulas, targets, diseases, symptoms, syndromes, evidence, and monographs.

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Disease: 1Target: 2Links: 2
Arranging relationship network...

Record Fields

Scalar fields from the final disease record.

Disease Id
14817
Core Entity Id
72661
Source Entity Count
1
Preferred Name
Spondyloepimetaphyseal Dysplasia, X-Linked
Name Cn
X连锁脊椎干骺端发育不良
Name Pinyin
X Lian Suo Ji Zhui Gan Hou Duan Fa Yu Bu Liang
Name En
Spondyloepimetaphyseal Dysplasia, X-Linked
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, X-Linked
Role
preferred
Name
SEMD, X-LINKED
Role
alias
Name
SEMDX
Role
alias

Cross References

Trusted external identifiers retained for this final record.

Herb
HBDIS016434
Omim
300106
Umls
C1848097
Sym Map
SMDE02408
Dis Ge Net
C1848097
Umls Sty
T047
Me Sh Class
C05C16
Tcmbank Disease
8431

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