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
- 15321
- Core Entity Id
- 73240
- Source Entity Count
- 1
- Preferred Name
- Metaphyseal Chondrodysplasia With Retinitis Pigmentosa
- Name Cn
- 干骺端软骨发育不良伴视网膜色素变性
- Name Pinyin
- Gan Hou Duan Ruan Gu Fa Yu Bu Liang Ban Shi Wang Mo Se Su Bian Xing
- Name En
- Metaphyseal Chondrodysplasia With Retinitis Pigmentosa
- Name Latin
- Bilingual Status
- complete
- Disease Type
- disease
- Umls Disease Type
- Disease or Syndrome
- Disgenet Type
- disease
- Mesh Class
- Eye Diseases; Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Musculoskeletal Diseases
- Do Class
- Hpo Class
- Mesh Class Name
- Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Eye Diseases; 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
Metaphyseal Chondrodysplasia With Retinitis Pigmentosa
Role
preferred
Name
Retinitis Pigmentosa With Or Without Skeletal Anomalies
Role
alias
Cross References
Trusted external identifiers retained for this final record.
Herb
HBDIS017117
Omim
250410
Umls
C1855188
Sym Map
SMDE04734
Dis Ge Net
C1855188
Umls Sty
T047
Me Sh Class
C05C11C16
Tcmbank Disease
28407
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
Eye Diseases; 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; Eye Diseases; Musculoskeletal Diseases
Umls Semantic Type Name
Disease or Syndrome