DiseaseID 16263

色素性静脉旁脉络膜视网膜萎缩

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: 1Links: 1
Arranging relationship network...

Record Fields

Scalar fields from the final disease record.

Disease Id
16263
Core Entity Id
74309
Source Entity Count
1
Preferred Name
Pigmented Paravenous Chorioretinal Atrophy
Name Cn
色素性静脉旁脉络膜视网膜萎缩
Name Pinyin
Se Su Xing Jing Mai Pang Mai Luo Mo Shi Wang Mo Wei Suo
Name En
Pigmented Paravenous Chorioretinal Atrophy
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
Do Class
Hpo Class
Mesh Class Name
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Eye 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
Pigmented Paravenous Chorioretinal Atrophy
Role
preferred
Name
PPCRA
Role
alias

Cross References

Trusted external identifiers retained for this final record.

Herb
HBDIS018432
Omim
172870
Umls
C1868310
Sym Map
SMDE00097
Dis Ge Net
C1868310
Umls Sty
T047
Me Sh Class
C11C16
Tcmbank Disease
28378

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
Dis Ge Net Disease Type
disease
Disease Class Name Me Sh
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Eye Diseases
Umls Semantic Type Name
Disease or Syndrome