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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
Osteopetrosis, Autosomal Recessive 7 (OPTB7)
Alias:
Autosomal Recessive Osteopetrosis 7
Autosomal Recessive Osteoclast-Poor Osteopetrosis with Hypogammaglobulinemia
Osteopetrosis-Hypogammaglobulinemia Syndrome
Autosomal Recessive Osteopetrosis Type 7
Optb7
Osteoclast-Poor Osteopetrosis with Hypogammaglobulinemia
Osteopetrosis, Osteoclast-Poor, with Hypogammaglobulinemia
Osteopetrosis, Autosomal Recessive, Type 7
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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
Osteopetrosis, Autosomal Recessive 7,也被称为常染色体隐性骨病7,与骨病和常染色体隐性骨病2有关。与Osteopetrosis, Autosomal Recessive 7相关的基因是TNFRSF11A(TNF受体超家族成员11a),其相关通路/超通路包括无机离子/氨基酸/寡肽的运输和受体酪氨酸激酶的信号传导。相关组织包括骨和骨髓,相关表型包括进行性视觉丧失和骨质增生。
Related ID:
MALACARDS:OST136
OMIM:612301
MESH:D010022
Basic Information
Inheritance
Age of Onset
Prevalence
Related Gene
Related Mouse Models
Reference
MALACARDS
常隐
新生儿
<1/1000000
6
53
3
OST136
Medical Symptom
#
Categorization
Description
HPO Frequency
Orphanet Frequency
HPO Source Accession
No data available
Gene & Mutation
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Gene
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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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