DiseaseID 18311

皮质酮还原酶缺乏症1型

disease

Back to Browse

Relationship Network

Interactive first-hop connections across herbs, ingredients, formulas, targets, diseases, symptoms, syndromes, evidence, and monographs.

Click a node to open it in a new tab
Disease: 1Formula: 5Symptom: 4Target: 18Links: 33
Arranging relationship network...

Record Fields

Scalar fields from the final disease record.

Disease Id
18311
Core Entity Id
76690
Source Entity Count
1
Preferred Name
Cortisone Reductase Deficiency 1
Name Cn
皮质酮还原酶缺乏症1型
Name Pinyin
Pi Zhi Tong Huan Yuan Mei Que Fa Zheng 1 Xing
Name En
Cortisone Reductase Deficiency 1
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,v2
Suppressed
No

Names

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

Name
Cortisone Reductase Deficiency 1
Role
preferred
Name
CORTRD1
Role
alias

Cross References

Trusted external identifiers retained for this final record.

Herb
HBDIS021715
Omim
604931
Umls
C3551716
Sym Map
SMDE01395
Do Class
DOID:630DOID:7
Dis Ge Net
C3551716
Umls Sty
T047
Etcm Disease
Cortisone Reductase Deficiency 1
Tcmbank Disease
26086
Itcmdb Generated
ITX-DISEASE-7AEFC2C5EAA7

Attributes

Merged source attributes and domain-specific metadata.

Version
v1,v2
Suppress
0
Page Title
Disease Cortisone Reductase Deficiency 1 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 1
Global Category
Genetic diseases;Metabolic diseases
Anatomical Category
Endocrine diseases
Dis Ge Net Disease Type
disease
Umls Semantic Type Name
Disease or Syndrome