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
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:

Basic Information

Inheritance
Age of Onset
Prevalence
Related Gene
Related Mouse Models
Reference
MALACARDS
常显
未知
--
11
102
16

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