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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
Enchondromatosis, Multiple, Ollier Type (ENCHOM)
Alias:
Ollier Disease
Enchondromatosis
Dyschondroplasia
Osteochondromatosis
Enchondromatosis with Haemangiomata
Multiple Cartilaginous Enchondroses
Hereditary Multiple Exostoses
Enchondromatosis, Multiple
Multiple Enchondromatosis
Enchondromatosis Multiple
Ollier's Syndrome
Maffucci Disease
Kast's Syndrome
Olliers Disease
Chondromatosis
Enchom
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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
成骨发育不良,多发性,奥利尔型,也称为奥利尔病,与外生骨疣,多发性,类型I和遗传性多发性骨软骨瘤有关,症状包括疼痛。与成骨发育不良,多发性,奥利尔型相关的基因是IDH1(NADP(+)异柠檬酸脱氢酶1),其相关通路/超级通路包括信号转导和卡马西平受体的前突触功能。药物异维A酸已在该疾病的背景下被提及。附属组织包括骨和肝,相关表型为血管瘤和微脑症。
Related ID:
MALACARDS:ENC044
OMIM:166000
MESH:D004687
Basic Information
Inheritance
Age of Onset
Prevalence
Related Gene
Related Mouse Models
Reference
MALACARDS
常显
孩童期
1-9/100000
32
510
16
ENC044
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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