Log In|Sign Up
ENCongenital Symblepharon
Favorite
Congenital Symblepharon is related to cryptophthalmos, unilateral or bilateral, isolated and fraser syndrome 1. An important gene associated with Congenital Symblepharon is FREM2 (FRAS1 Related Extracellular Matrix 2). Affiliated tissues include eye and skin, and related phenotypes are growth/size/body region and embryo
Related ID：
Basic Information
Inheritance
Age of Onset
Prevalence
Related Gene
Related Mouse Models
Reference
MALACARDS
Medical Symptom
#
Categorization
Description
HPO Frequency
Orphanet Frequency
HPO Source Accession
Gene & Mutation
#
Gene
Function
Score
Mutations
Related Drugs
Name
CAS Number
Status
Phase
Disease Model
Category
Name
MGI
Related Gene
Strain of Origin
Publications
References Literature
Title
PMID
Journal
Year
IF
