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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
Peripheral Demyelinating Neuropathy, Central Dysmyelination, Waardenburg Syndrome, and Hirschsprung Disease (PCWH)
Alias:
Pcwh Syndrome
Pcwh
Neurologic Waardenburg-Shah Syndrome
Peripheral Demyelinating Neuropathy, Central Dysmyelinating Leukodystrophy, Waardenburg Syndrome and Hirschsprung Disease
Peripheral Demyelinating Neuropathy-Central Dysmyelinating Leukodystrophy-Hirschsprung Disease-Waardenburg Syndrome
Peripheral Demyelinating Neuropathy-Central Dysmyelinating Leukodystrophy-Waardenburg Syndrome-Hirschsprung Disease
Waardenburg-Shah Syndrome, Neurologic Variant
Waardenburg-Shah Syndrome Neurologic Variant
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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
周围脱髓鞘神经病、中央脱髓鞘、瓦登伯格综合症和希尔斯普龙病,也被称为PCWH综合症,与瓦登伯格综合症2b型和瓦登伯格综合症3型有关,症状包括共济失调和偏瘫、痉挛。与周围脱髓鞘神经病、中央脱髓鞘、瓦登伯格综合症和希尔斯普龙病有关的重要基因是SOX10(SRY-Box转录因子10),其相关通路/超级通路包括初级卵巢功能不全和前列腺素合成和调节。相关组织包括皮肤和嗅球,相关表型包括智力障碍和癫痫。
Related ID:
MALACARDS:PRP066
OMIM:609136
MESH:D006627
Basic Information
Inheritance
Age of Onset
Prevalence
Related Gene
Related Mouse Models
Reference
MALACARDS
常显
新生儿
<1/1000000
23
324
11
PRP066
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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