DiseaseID 12488

可的松还原酶缺乏症

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: 4Links: 5
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Record Fields

Scalar fields from the final disease record.

Disease Id
12488
Core Entity Id
70006
Source Entity Count
1
Preferred Name
Cortisone Reductase Deficiency
Name Cn
可的松还原酶缺乏症
Name Pinyin
Ke Di Song Huan Yuan Mei Que Fa Zheng
Name En
Cortisone Reductase Deficiency
Name Latin
Bilingual Status
complete
Disease Type
disease
Umls Disease Type
Disease or Syndrome
Disgenet Type
disease
Mesh Class
Endocrine System Diseases; Female Urogenital Diseases and Pregnancy Complications; Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases; Skin and Connective Tissue Diseases; Male Urogenital Diseases; Pathological Conditions, Signs and Symptoms
Do Class
disease of anatomical entity
Hpo Class
Mesh Class Name
Pathological Conditions, Signs and Symptoms; Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases; Female Urogenital Diseases and Pregnancy Complications; Skin and Connective Tissue Diseases; Male Urogenital Diseases; Endocrine System Diseases
Hpo Class Name
Do Class Name
disease of anatomical entity
Disease Definition
Version
v2
Suppressed
No

Names

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

Name
Cortisone Reductase Deficiency
Role
preferred

Cross References

Trusted external identifiers retained for this final record.

Herb
HBDIS013253
Umls
C1291245
Sym Map
SMDE07592
Do Class
DOID:7
Dis Ge Net
C1291245
Umls Sty
T047
Me Sh Class
C12C13C16C17C18C19C23
Tcmbank Disease
2014

Attributes

Merged source attributes and domain-specific metadata.

Version
v2
Suppress
0
Do Class Name
disease of anatomical entity
Disease Type
disease
Do Disease Class
disease of anatomical entity
Umls Disease Type
Disease or Syndrome
Me Sh Disease Class
Endocrine System Diseases; Female Urogenital Diseases and Pregnancy Complications; Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases; Skin and Connective Tissue Diseases; Male Urogenital Diseases; Pathological Conditions, Signs and Symptoms
Dis Ge Net Disease Type
disease
Disease Class Name Me Sh
Pathological Conditions, Signs and Symptoms; Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases; Female Urogenital Diseases and Pregnancy Complications; Skin and Connective Tissue Diseases; Male Urogenital Diseases; Endocrine System Diseases
Umls Semantic Type Name
Disease or Syndrome