DiseaseID 200

皮质酮还原酶缺乏症2型

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: 1Target: 18Links: 25
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Record Fields

Scalar fields from the final disease record.

Disease Id
200
Core Entity Id
225
Source Entity Count
1
Preferred Name
Cortisone Reductase Deficiency 2
Name Cn
皮质酮还原酶缺乏症2型
Name Pinyin
Pi Zhi Tong Huan Yuan Mei Que Fa Zheng 2 Xing
Name En
Cortisone Reductase Deficiency 2
Name Latin
Bilingual Status
complete
Disease Type
disease
Umls Disease Type
Disease or Syndrome
Disgenet Type
disease
Mesh Class
Do Class
disease of anatomical entity; genetic disease
Hpo Class
Mesh Class Name
Hpo Class Name
Do Class Name
genetic disease; disease of anatomical entity
Disease Definition
Version
v1
Suppressed
No

Names

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

Name
Cortisone Reductase Deficiency 2
Role
preferred
Name
11-Beta-Hydroxysteroid Dehydrogenase Type 1 Deficiency
Role
preferred
Name
CORTRD2
Role
alias

Cross References

Trusted external identifiers retained for this final record.

Herb
HBDIS021753HBDIS026496
Omim
614662
Umls
C3553382
Sym Map
SMDE01368
Do Class
DOID:630DOID:7
Dis Ge Net
C3553382C4329210
Umls Sty
T047
Etcm Disease
Cortisone Reductase Deficiency 2
Tcmbank Disease
1484127249
Itcmdb Generated
ITX-DISEASE-643A70EA37B7

Attributes

Merged source attributes and domain-specific metadata.

Version
v1
Suppress
0
Page Title
Disease Cortisone Reductase Deficiency 2 Details page
Do Class Name
genetic disease; disease of anatomical entity
Disease Type
disease
Do Disease Class
disease of anatomical entity; genetic disease
Umls Disease Type
Disease or Syndrome
Basic Information
Disease Name
Cortisone Reductase Deficiency 2
Global Category
Genetic diseases;Metabolic diseases
Anatomical Category
Endocrine diseases
Dis Ge Net Disease Type
disease
Umls Semantic Type Name
Disease or Syndrome