Congenital Nystagmus

Alias:
Nystagmus, Congenital
Nystagmus Congenital
Favorite
Basic Information
Medical Symptom
Gene & Mutation
Related Drugs
Disease Model
References Literature
Congenital Nystagmus, also known as nystagmus, congenital, is related to nystagmus 7, congenital, autosomal dominant and nystagmus 6, congenital, x-linked, and has symptoms including deficiencies of smooth pursuit movements An important gene associated with Congenital Nystagmus is FRMD7 (FERM Domain Containing 7), and among its related pathways/superpathways are Visual Cycle in Retinal Rods and Visual signal transduction: Cones. Affiliated tissues include eye and brain, and related phenotypes are Decreased human papilloma virus 16 (HPV16) pseudovirus infection and cellular
Related ID:
MESH:D020417

Basic Information

Inheritance
Age of Onset
Prevalence
Related Gene
Related Mouse Models
Reference
MALACARDS
--
Unknown
--
22
285
--

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