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COL4A5 c.1390G>A
ALS1
DMD c.1332-11868C>G
TP53
肌萎缩侧索硬化症1型
USH2A c.8559-2A>G
囊性纤维化
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中文
罕见病
Alkaptonuria (AKU)
Alias:
Homogentisic Acid Oxidase Deficiency
Alcaptonuria
Aku
Homogentisate 1,2-Dioxygenase Deficiency
Deficiency of Homogentisicase
Ochronosis, Hereditary
Hereditary Ochronosis
Deficiency of Homogentisate Oxygenase
Alkaptonuric Ochronosis
Homogentisic Acidura
Homogentisicaciduria
Ochronosis
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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
阿尔卡酮尿症,也被称为同庚酸氧化酶缺乏症,与褐黄病和腹部肥胖-代谢综合征1有关,其症状包括背痛。与阿尔卡酮尿症相关的重要基因是HGD(同庚酸1,2-二氧醇酶),其相关通路/超级通路包括代谢和SLITs和ROBOs的表达调控。在该疾病的背景下提到了尼替尼酮和酶抑制剂。附属组织包括皮肤和眼睛,相关表型为关节炎和关节僵硬。
Related ID:
MALACARDS:ALK013
OMIM:203500
MESH:D000474
ICD11:1761652827
Basic Information
Inheritance
Age of Onset
Prevalence
Related Gene
Related Mouse Models
Reference
MALACARDS
常隐
婴儿期
1-9/100000
17
258
97
ALK013
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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