DiseaseID 7549

皮质酮甲基氧化酶I型缺乏症

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: 2Target: 1Links: 3
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Record Fields

Scalar fields from the final disease record.

Disease Id
7549
Core Entity Id
64361
Source Entity Count
1
Preferred Name
Corticosterone Methyl Oxidase Type I Deficiency
Name Cn
皮质酮甲基氧化酶I型缺乏症
Name Pinyin
Pi Zhi Tong Jia Ji Yang Hua Mei I Xing Que Fa Zheng
Name En
Corticosterone Methyl Oxidase Type I Deficiency
Name Latin
Bilingual Status
complete
Disease Type
disease
Umls Disease Type
Disease or Syndrome
Disgenet Type
disease
Mesh Class
Endocrine System Diseases
Do Class
Hpo Class
Mesh Class Name
Endocrine 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
Corticosterone Methyl Oxidase Type I Deficiency
Role
preferred
Name
Corticosterone Methyloxidase Type I Deficiency
Role
preferred
Name
18-HYDROXYLASE DEFICIENCY
Role
alias
Name
ALDOSTERONE DEFICIENCY DUE TO DEFECT IN STEROID 18-HYDROXYLASE
Role
alias
Name
ALDOSTERONE DEFICIENCY I
Role
alias
Name
Aldosterone Deficiency Due To Defect In 18-Hydroxylase
Role
alias
Name
CMO I DEFICIENCY
Role
alias
Name
FHHA1A
Role
alias
Name
HYPERRENINEMIC HYPOALDOSTERONISM, FAMILIAL, 1
Role
alias
Name
STEROID 18-HYDROXYLASE DEFICIENCY
Role
alias

Cross References

Trusted external identifiers retained for this final record.

Herb
HBDIS006247
Omim
203400
Umls
C0268293
Sym Map
SMDE03631
Dis Ge Net
C0268293
Umls Sty
T047
Me Sh Class
C19
Tcmbank Disease
5881

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
Endocrine System Diseases
Dis Ge Net Disease Type
disease
Disease Class Name Me Sh
Endocrine System Diseases
Umls Semantic Type Name
Disease or Syndrome