DiseaseID 26520
先天性红细胞生成性卟啉症
Congenital Erythropoietic Porphyria
Congenital erythropoietic porphyria, or Günther disease, is a form of erythropoietic porphyria characterized by very severe and mutilating photodermatosis.
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Disease: 1Symptom: 3Target: 2Links: 5
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Record Fields
Scalar fields from the final disease record.
- Disease Id
- 26520
- Core Entity Id
- 119088
- Source Entity Count
- 1
- Preferred Name
- Congenital Erythropoietic Porphyria
- Name Cn
- 先天性红细胞生成性卟啉症
- Name Pinyin
- Xian Tian Xing Hong Xi Bao Sheng Cheng Xing Bu Lin Zheng
- Name En
- Congenital Erythropoietic Porphyria
- 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
- Congenital erythropoietic porphyria, or Günther disease, is a form of erythropoietic porphyria characterized by very severe and mutilating photodermatosis.
- Version
- v1
- Suppressed
- No
Names
Preferred names, aliases, and source labels retained in the final schema.
Name
Congenital Erythropoietic Porphyria
Role
preferred
Source
SymMap_v2
Preferred
Yes
Cross References
Trusted external identifiers retained for this final record.
Sym Map
SMDE03887
Orphanet
79277
Attributes
Merged source attributes and domain-specific metadata.
Version
v1
Suppress
0
Disease Definition
Congenital erythropoietic porphyria, or Günther disease, is a form of erythropoietic porphyria characterized by very severe and mutilating photodermatosis.