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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
Neuropathy, Hereditary, with Liability to Pressure Palsies (HNPP)
Alias:
Tomaculous Neuropathy
Hereditary Neuropathy with Liability to Pressure Palsies
Hnpp
Current Pressure-Sensitive Neuropathy
Heterozygous Microdeletion 17p11.2p12
Tulip-Bulb Digger's Palsy
Potato-Grubbing Palsy
Neuropathy, Recurrent, with Pressure Palsies
Hereditary Liability to Pressure Palsies
Familial Recurrent Polyneuropathy
Entrapment Neuropathies
Neuropathy Hereditary with Liability to Pressure Palsies
Neuropathy, Hereditary, with Liability Pressure Palsies
Hereditary Motor and Sensory Neuropathies
Hereditary Pressure Sensitive Neuropathy
Hereditary Motor and Sensory Neuropathy
Familial Pressure Sensitive Neuropathy
Inherited Tendency to Pressure Palsies
Polyneuropathy, Familial Recurrent
Nerve Compression Syndrome
Compression Neuropathy
Entrapment Neuropathy
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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
遗传性神经病变,易感压力性瘫痪,又称汤马丘神经病变,与Charcot-Marie-Tooth病,轴突型2a1和Charcot-Marie-Tooth病1g有关,症状包括神经痛。与遗传性神经病变,易感压力性瘫痪有关的重要基因是PMP22(周围髓蛋白22),其相关通路/超级通路包括参与CMT神经病变的细胞内转运蛋白质和EGR2和SOX10介导的施万细胞髓鞘化。在该疾病的背景下,已提到的药物有叶酸和硫辛酸。附属组织包括脊髓和大脑,相关表型为周围神经病变和运动神经传导速度降低。
Related ID:
MALACARDS:NRP051
OMIM:162500
MESH:C536965
Basic Information
Inheritance
Age of Onset
Prevalence
Related Gene
Related Mouse Models
Reference
MALACARDS
常显
婴儿期
1-5/10000
24
212
68
NRP051
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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