Acth Deficiency, Isolated (IAD)

Alias:
Adrenocorticotropic Hormone Deficiency
Iad
Congenital Isolated Adrenocorticotropic Hormone Deficiency
Adrenocorticotropic Hormone [acth] Deficiency
Adrenocorticotropic Hormone Deficiency
Secondary Adrenocortical Insufficiency
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基础信息
疾病表征
基因 & 突变
靶点药物
疾病模型
文献报道
ACTH缺乏症,孤立型,也称为促肾上腺皮质激素缺乏症,与早发性卵巢功能不全7和不适当的ADH综合征有关。与ACTH缺乏症,孤立型有关的重要基因是TBX19(T-Box转录因子19),其相关通路/超级通路包括促肾上腺皮质激素信号通路和糖皮质激素受体调节网络。附属组织包括垂体和肾上腺皮质,相关表型包括癫痫和黄疸。
Related ID:
MESH:C535668
ICD11:538301537

Basic Information

Inheritance
Age of Onset
Prevalence
Related Gene
Related Mouse Models
Reference
MALACARDS
常隐
新生儿
--
14
111
16

Medical Symptom

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Categorization
Description
HPO Frequency
Orphanet Frequency
HPO Source Accession
No data available

Gene & Mutation

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Gene
Function
Score
Mutations
No data available

Related Drugs

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CAS Number
Status
Phase
No data available

Disease Model

Category
Name
MGI
Related Gene
Strain of Origin
Publications
No data available

References Literature

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PMID
Journal
Year
IF
No Data Found!
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