Home
Toolbox
Resource
Workflow
Tutorials
Citations
Downloads
Mutation Al-Predictor Flow
Gene-to-Mutation Flow
News & Insights
Genetic Encyclopedia
Frontiers
Industry Insights
Case Studies
About Us
About the Site
Contact Us
Private Policy
User Agreement
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
Log In
|
Sign Up
中文
罕见病
Clubfoot, Congenital, with or Without Deficiency of Long Bones and/or Mirror-Image Polydactyly (CCF)
Alias:
Familial Clubfoot Due to 5q31 Microdeletion
Ccf
Clubfoot, Congenital, with/without Deficiency of Long Bones and/or Mirror-Image Polydactyly
Hereditary Clubfoot Due to Pitx1 Point Mutation
Familial Clubfoot Due to Pitx1 Point Mutation
Hereditary Clubfoot Due to 5q31 Microdeletion
Talipes Equinovarus
Clubfoot
Tev
新建收藏夹
取消
确认
加入收藏夹
选择一个收藏夹
描述信息
新收藏夹 >>
取消
确认
加入收藏
基础信息
疾病表征
基因 & 突变
靶点药物
疾病模型
文献报道
先天性马蹄内翻足,伴有或不伴有长骨和/或镜像多指,也称为5q31微缺失引起的家族性马蹄内翻足,与远端关节挛缩和多指有关。与先天性马蹄内翻足,伴有或不伴有长骨和/或镜像多指相关的基因是PITX1(配对同源域1),其相关通路/超通路包括离子通道转运。在该疾病的背景下,氯硝西泮和利多卡因已被提及。相关组织包括骨和骨骼肌,相关表型为矮小和双侧马蹄内翻足。
Related ID:
MALACARDS:CLB019
OMIM:119800
MESH:D003025
Basic Information
Inheritance
Age of Onset
Prevalence
Related Gene
Related Mouse Models
Reference
MALACARDS
常显
未知
--
11
102
16
CLB019
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!
微信
信息比对
科研助手
使用教程
回到顶部