Reducing Body Myopathy, X-Linked 1b, with Late Childhood or Adult Onset (RBMX1B)

Alias:
Rbmx1b
Myopathy, Reducing Body, X-Linked, Childhood-Onset
Myopathy, Reducing Body, X-Linked, Type 1b
Favorite
Basic Information
Medical Symptom
Gene & Mutation
Related Drugs
Disease Model
References Literature
Reducing Body Myopathy, X-Linked 1b, with Late Childhood or Adult Onset, also known as rbmx1b, is related to reducing body myopathy, x-linked 1a, severe, with infantile or early childhood onset. An important gene associated with Reducing Body Myopathy, X-Linked 1b, with Late Childhood or Adult Onset is FHL1 (Four And A Half LIM Domains 1). Affiliated tissues include skeletal muscle, and related phenotypes are scoliosis and flexion contracture
Related ID:

Basic Information

Inheritance
Age of Onset
Prevalence
Related Gene
Related Mouse Models
Reference
MALACARDS
XLD
XL
XLR
Unknown
--
1
5
7

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!
Wechat
Comparison
Al agent
Tutorials
Back to top