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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
Focal Dermal Hypoplasia (FDH)
Alias:
Goltz Syndrome
Goltz-Gorlin Syndrome
Fodh
Fdh
Dhof
Hypoplasia, Dermal, Focal
Goltz Gorlin Syndrome
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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
焦点性真皮发育不良,又名戈尔茨综合症,与手足分裂畸形和黄斑裂孔有关。与焦点性真皮发育不良有关的重要基因是 PORCN (Porcupine O-Acyltransferase),其相关通路/超级通路包括信号转导和 GPCR 下游信号转导。附属组织包括皮肤和眼睛,相关表型包括听力障碍和指甲异常。
Related ID:
MALACARDS:FCL009
OMIM:305600
MESH:D005489
Basic Information
Inheritance
Age of Onset
Prevalence
Related Gene
Related Mouse Models
Reference
MALACARDS
X染色体
X隐
新生儿
<1/1000000
22
301
42
FCL009
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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