Combined Pituitary Hormone Deficiencies, Genetic Forms

Alias:
Multiple Pituitary Hormone Deficiencies, Genetic Forms
Combined Pituitary Hormone Deficiencies, Genetic Form
Familial Congenital Hypopituitarism
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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
复合垂体激素缺乏症,遗传型,又称多垂体激素缺乏症,遗传型,与垂体功能减退症和垂体激素缺乏症有关,复合,2。与复合垂体激素缺乏症,遗传型有关的重要基因是PROP1(PROP配对样同源盒1),其相关通路/超级通路包括胚胎和诱导多能干细胞和特异性标记物和内胚层分化。附属组织包括垂体和眼睛,相关表型为垂体功能减退症和低血压。
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Basic Information

Inheritance
Age of Onset
Prevalence
Related Gene
Related Mouse Models
Reference
MALACARDS
X显
常显
常隐
X染色体
全年龄段
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7
109
21

Medical Symptom

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

Gene & Mutation

#
Gene
Function
Score
Mutations
No data available

Related Drugs

Name
CAS Number
Status
Phase
No data available

Disease Model

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

References Literature

Title
PMID
Journal
Year
IF
No Data Found!
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