DiseaseID 14750

低前β脂蛋白血症、棘红细胞增多症、视网膜色素变性及苍白球变性

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: 1Symptom: 2Target: 2Links: 4
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Record Fields

Scalar fields from the final disease record.

Disease Id
14750
Core Entity Id
72585
Source Entity Count
1
Preferred Name
Hypoprebetalipoproteinemia, Acanthocytosis, Retinitis Pigmentosa, And Pallidal Degeneration
Name Cn
低前β脂蛋白血症、棘红细胞增多症、视网膜色素变性及苍白球变性
Name Pinyin
Di Qian Β Zhi Dan Bai Xue Zheng 、 Ji Hong Xi Bao Zeng Duo Zheng 、 Shi Wang Mo Se Su Bian Xing Ji Cang Bai Qiu Bian Xing
Name En
Hypoprebetalipoproteinemia, Acanthocytosis, Retinitis Pigmentosa, And Pallidal Degeneration
Name Latin
Bilingual Status
complete
Disease Type
disease
Umls Disease Type
Disease or Syndrome
Disgenet Type
disease
Mesh Class
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nervous System Diseases
Do Class
Hpo Class
Mesh Class Name
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nervous System Diseases
Hpo Class Name
Do Class Name
Disease Definition
Version
v1,v2
Suppressed
No

Names

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

Name
Hypoprebetalipoproteinemia, Acanthocytosis, Retinitis Pigmentosa, And Pallidal Degeneration
Role
preferred
Name
HARP SYNDROME
Role
alias

Cross References

Trusted external identifiers retained for this final record.

Herb
HBDIS016342
Omim
607236
Umls
C1846582
Sym Map
SMDE03649
Dis Ge Net
C1846582
Umls Sty
T047
Me Sh Class
C10C16
Tcmbank Disease
31751

Attributes

Merged source attributes and domain-specific metadata.

Version
v1,v2
Suppress
0
Disease Type
disease
Umls Disease Type
Disease or Syndrome
Me Sh Disease Class
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nervous System Diseases
Dis Ge Net Disease Type
disease
Disease Class Name Me Sh
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nervous System Diseases
Umls Semantic Type Name
Disease or Syndrome