Anterior Segment Dysgenesis Gene Set

Dataset DisGeNET Gene-Disease Associations
Category disease or phenotype associations
Type disease
Description Abnormal development (dysgenesis) of the anterior segment of the eye globe. These structures are mainly of mesenchymal origin. (Human Phenotype Ontology, HP_0007700)
External Link https://www.disgenet.org/browser/0/1/0/C3151617
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Genes

12 genes associated with the disease Anterior Segment Dysgenesis in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.

Symbol Name
ATOH7 atonal homolog 7 (Drosophila)
CPAMD8 C3 and PZP-like, alpha-2-macroglobulin domain containing 8
CYP1B1 cytochrome P450, family 1, subfamily B, polypeptide 1
ELP4 elongator acetyltransferase complex subunit 4
FOXC1 forkhead box C1
FOXE3 forkhead box E3
PAX6 paired box 6
PITX2 paired-like homeodomain 2
PITX3 paired-like homeodomain 3
PTCH1 patched 1
PXDN peroxidasin
TSC1 tuberous sclerosis 1