Log In|Sign Up
ENAural Atresia, Congenital (CAA)
Alias:
Aural Atresia, Congenital, with Hyposmia
Caa
Favorite
Aural Atresia, Congenital, also known as caa, is related to cerebral amyloid angiopathy, cst3-related and cerebral amyloid angiopathy, app-related. An important gene associated with Aural Atresia, Congenital is TSHZ1 (Teashirt Zinc Finger Homeobox 1). Affiliated tissues include olfactory bulb, and related phenotypes are conductive hearing impairment and atresia of the external auditory canal
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
