DiseaseID 26501

先天性肾上腺发育不良

Adrenal Hypoplasia, Congenital

NCI2016_02D:A rare genetic disorder that affects the adrenal gland. It usually presents in infancy with signs and symptoms of adrenal insufficiency. If it is not recognized and treated promptly, it may be lethal.|HPO2016

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Relationship Network

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Disease: 1Formula: 9Herb: 2Target: 22Links: 35
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Record Fields

Scalar fields from the final disease record.

Disease Id
26501
Core Entity Id
119069
Source Entity Count
1
Preferred Name
Adrenal Hypoplasia, Congenital
Name Cn
先天性肾上腺发育不良
Name Pinyin
Xian Tian Xing Shen Shang Xian Fa Yu Bu Liang
Name En
Adrenal Hypoplasia, Congenital
Name Latin
Bilingual Status
complete
Disease Type
Umls Disease Type
Disgenet Type
Mesh Class
Do Class
Hpo Class
Mesh Class Name
Hpo Class Name
Do Class Name
Disease Definition
NCI2016_02D:A rare genetic disorder that affects the adrenal gland. It usually presents in infancy with signs and symptoms of adrenal insufficiency. If it is not recognized and treated promptly, it may be lethal.|HPO2016_07_04:A type of adrenal hypoplasia with congenital onset. [HPO:probinson]
Version
v1
Suppressed
No

Names

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

Name
Adrenal Hypoplasia, Congenital
Role
preferred

Cross References

Trusted external identifiers retained for this final record.

Umls
C0220766C0342482
Sym Map
SMDE03773
Etcm Disease
Adrenal Hypoplasia, Congenital
Itcmdb Generated
ITX-DISEASE-FF03BEFC846D

Attributes

Merged source attributes and domain-specific metadata.

Version
v1
Suppress
0
Page Title
Disease Adrenal Hypoplasia, Congenital Details page
Basic Information
Disease Name
Adrenal Hypoplasia, Congenital
Global Category
Genetic diseases;Rare diseases
Anatomical Category
Endocrine diseases;Reproductive diseases
Disease Definition
NCI2016_02D:A rare genetic disorder that affects the adrenal gland. It usually presents in infancy with signs and symptoms of adrenal insufficiency. If it is not recognized and treated promptly, it may be lethal.|HPO2016_07_04:A type of adrenal hypoplasia with congenital onset. [HPO:probinson]