DiseaseID 25861
遗传性热异形红细胞症
Pyropoikilocytosis, Hereditary
NCI2016_02D:An autosomal recessive inherited severe hemolytic anemia. It is a subtype of hereditary elliptocytosis and is characterized by partial spectrin deficiency.|HPO2016_07_04:A form of severe hemolytic anemia char
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Disease: 1Target: 2Links: 2
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Record Fields
Scalar fields from the final disease record.
- Disease Id
- 25861
- Core Entity Id
- 118429
- Source Entity Count
- 1
- Preferred Name
- Pyropoikilocytosis, Hereditary
- Name Cn
- 遗传性热异形红细胞症
- Name Pinyin
- Yi Chuan Xing Re Yi Xing Hong Xi Bao Zheng
- Name En
- Pyropoikilocytosis, Hereditary
- 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
- NCI2016_02D:An autosomal recessive inherited severe hemolytic anemia. It is a subtype of hereditary elliptocytosis and is characterized by partial spectrin deficiency.|HPO2016_07_04:A form of severe hemolytic anemia characterized by erythrocyte morphology reminiscent of that seen in patients after a thermal burn. [HPO:probinson, pmid:16304353]
- Version
- v1
- Suppressed
- No
Names
Preferred names, aliases, and source labels retained in the final schema.
Name
Pyropoikilocytosis, Hereditary
Role
preferred
Source
SymMap_v2
Preferred
Yes
Cross References
Trusted external identifiers retained for this final record.
Umls
C0520739
Sym Map
SMDE00700
Attributes
Merged source attributes and domain-specific metadata.
Version
v1
Suppress
0
Disease Definition
NCI2016_02D:An autosomal recessive inherited severe hemolytic anemia. It is a subtype of hereditary elliptocytosis and is characterized by partial spectrin deficiency.|HPO2016_07_04:A form of severe hemolytic anemia characterized by erythrocyte morphology reminiscent of that seen in patients after a thermal burn. [HPO:probinson, pmid:16304353]