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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
Encephalopathy, Progressive, Early-Onset, with Brain Edema and/or Leukoencephalopathy, 2 (PEBEL2)
Alias:
Nad Hx Dehydratase Deficiency
Pebel2
Encephalopathy, Progressive, Early-Onset, with Brain Edema and/or Leukoencephalopathy, Type 2
Carkd Deficiency
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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
脑积水,早期进展型,伴有脑水肿和/或白质脑病2,也被称为NADHX缺乏症。与脑积水,早期进展型,伴有脑水肿和/或白质脑病2相关的基因是NAXD(NAD(P)HX脱水酶)。相关组织包括大脑和皮肤,相关表型为皮疹和脑病。
Related ID:
MALACARDS:ENC066
OMIM:618321
MESH:D020271
Basic Information
Inheritance
Age of Onset
Prevalence
Related Gene
Related Mouse Models
Reference
MALACARDS
常隐
婴儿期
<1/1000000
1
4
5
ENC066
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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