DiseaseID 18144

皮质酮甲基氧化酶II型缺乏症

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: 1Target: 2Links: 2
Arranging relationship network...

Record Fields

Scalar fields from the final disease record.

Disease Id
18144
Core Entity Id
76495
Source Entity Count
1
Preferred Name
Corticosterone Methyl Oxidase Type Ii Deficiency
Name Cn
皮质酮甲基氧化酶II型缺乏症
Name Pinyin
Pi Zhi Tong Jia Ji Yang Hua Mei Ii Xing Que Fa Zheng
Name En
Corticosterone Methyl Oxidase Type Ii Deficiency
Name Latin
Bilingual Status
complete
Disease Type
disease
Umls Disease Type
Disease or Syndrome
Disgenet Type
disease
Mesh Class
Do Class
Hpo Class
Mesh Class Name
Hpo Class Name
Do Class Name
Disease Definition
Version
v1
Suppressed
No

Names

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

Name
Corticosterone Methyl Oxidase Type Ii Deficiency
Role
preferred
Name
Corticosterone Methyloxidase Type Ii Deficiency
Role
preferred
Name
18-OXIDASE DEFICIENCY
Role
alias
Name
ALDOSTERONE DEFICIENCY DUE TO DEFICIENCY OF STEROID 18-OXIDASE
Role
alias
Name
ALDOSTERONE DEFICIENCY II
Role
alias
Name
CMO II DEFICIENCY
Role
alias
Name
FHHA1B
Role
alias
Name
HYPERRENINEMIC HYPOALDOSTERONISM, FAMILIAL, 1
Role
alias
Name
STEROID 18-OXIDASE DEFICIENCY
Role
alias

Cross References

Trusted external identifiers retained for this final record.

Herb
HBDIS021403
Omim
610600
Umls
C3463917
Sym Map
SMDE01888
Dis Ge Net
C3463917
Umls Sty
T047
Tcmbank Disease
31911

Attributes

Merged source attributes and domain-specific metadata.

Version
v1
Suppress
0
Disease Type
disease
Umls Disease Type
Disease or Syndrome
Dis Ge Net Disease Type
disease
Umls Semantic Type Name
Disease or Syndrome