Jalili Syndrome (JALIS)

Alias:
Cone Rod Dystrophy-Amelogenesis Imperfecta Syndrome
Cone-Rod Dystrophy and Amelogenesis Imperfecta
Cone Rod Dystrophy Amelogenesis Imperfecta
Jalis
Favorite
Basic Information
Medical Symptom
Gene & Mutation
Related Drugs
Disease Model
References Literature
Jalili Syndrome, also known as cone rod dystrophy-amelogenesis imperfecta syndrome, is related to dental caries and amelogenesis imperfecta, and has symptoms including photophobia An important gene associated with Jalili Syndrome is CNNM4 (Cyclin And CBS Domain Divalent Metal Cation Transport Mediator 4), and among its related pathways/superpathways are Regulation of Insulin-like Growth Factor (IGF) transport and uptake by Insulin-like Growth Factor Binding Proteins (IGFBPs) and 2q11.2 copy number variation syndrome. Affiliated tissues include eye and retina, and related phenotypes are nystagmus and visual impairment
Related ID:

Basic Information

Inheritance
Age of Onset
Prevalence
Related Gene
Related Mouse Models
Reference
MALACARDS
AR
Child
1-9/100000
15
83
6

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