Immunodeficiency-Centromeric Instability-Facial Anomalies Syndrome 2 (ICF2)

Alias:
Icf2
Immunodeficiency-Centromeric Instability-Facial Anomalies Syndrome, Type 2
Icf Syndrome 2
Favorite
Basic Information
Medical Symptom
Gene & Mutation
Related Drugs
Disease Model
References Literature
Immunodeficiency-Centromeric Instability-Facial Anomalies Syndrome 2, also known as icf2, is related to immunodeficiency-centromeric instability-facial anomalies syndrome and immune deficiency disease. An important gene associated with Immunodeficiency-Centromeric Instability-Facial Anomalies Syndrome 2 is ZBTB24 (Zinc Finger And BTB Domain Containing 24). Affiliated tissues include b cells and lung, and related phenotype is vision/eye.
Related ID:

Basic Information

Inheritance
Age of Onset
Prevalence
Related Gene
Related Mouse Models
Reference
MALACARDS
AR
Unknown
--
3
28
18

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