Anterior Segment Dysgenesis 7 (ASGD7)

Alias:
Corneal Opacification with Other Ocular Anomalies
Sclerocornea with Other Ocular Anomalies
Asgd7
Copoa
Dysgenesis, Anterior Segment, with Sclerocornea , Type 7
Congenital Cataract Microcornea with Corneal Opacity
Anterior Segment Dysgenesis 7, with Sclerocornea
Ccmco
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Basic Information
Medical Symptom
Gene & Mutation
Related Drugs
Disease Model
References Literature
Anterior Segment Dysgenesis 7, also known as corneal opacification with other ocular anomalies, is related to anterior segment dysgenesis and cataract. An important gene associated with Anterior Segment Dysgenesis 7 is PXDN (Peroxidasin). Affiliated tissues include eye, and related phenotypes are cataract and corneal opacity
Related ID:

Basic Information

Inheritance
Age of Onset
Prevalence
Related Gene
Related Mouse Models
Reference
MALACARDS
AR
Newborn
--
2
18
7

Medical Symptom

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Categorization
Description
HPO Frequency
Orphanet Frequency
HPO Source Accession
No data available

Gene & Mutation

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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
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