DiseaseID 26529

视网膜血管病伴脑白质脑病及全身表现

Retinal Vasculopathy With Cerebral Leukoencephalopathy And Systemic Manifestations

Retinal vasculopathy and cerebral leukodystrophy (RVCL) is an inherited group of small vessel diseases comprised of cerebroretinal vasculopathy (CRV), hereditary vascular retinopathy (HRV) and heredit

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Disease: 1Symptom: 11Target: 4Links: 15

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Record Fields

Scalar fields from the final disease record.

Disease Id: 26529
Core Entity Id: 119097
Source Entity Count: 1
Preferred Name: Retinal Vasculopathy With Cerebral Leukoencephalopathy And Systemic Manifestations
Name Cn: 视网膜血管病伴脑白质脑病及全身表现
Name Pinyin: Shi Wang Mo Xue Guan Bing Ban Nao Bai Zhi Nao Bing Ji Quan Shen Biao Xian
Name En: Retinal Vasculopathy With Cerebral Leukoencephalopathy And Systemic Manifestations
Name Latin
Bilingual Status: complete
Disease Type
Umls Disease Type
Disgenet Type
Mesh Class
Do Class
Hpo Class
Mesh Class Name
Hpo Class Name
Do Class Name
Disease Definition: Retinal vasculopathy and cerebral leukodystrophy (RVCL) is an inherited group of small vessel diseases comprised of cerebroretinal vasculopathy (CRV), hereditary vascular retinopathy (HRV) and heredit
Version: v1,v2
Suppressed: No

Names

Preferred names, aliases, and source labels retained in the final schema.

Name

Retinal Vasculopathy With Cerebral Leukoencephalopathy And Systemic Manifestations

Role

preferred

Source

SymMap_v2

Preferred

Yes

Cross References

Trusted external identifiers retained for this final record.

Umls

C1860518

Sym Map

SMDE03939

Orphanet

247691

Attributes

Merged source attributes and domain-specific metadata.

Version

v1,v2

Suppress

Disease Definition