Microphthalmia, Syndromic 3 [Supplementary Concept]
PROM mutation in SOX2
Date introduced: November 5, 2012
MeSH Unique ID: C565948
Heading Mapped to:
Entry Terms:
- Microphthalmia And Esophageal Atresia Syndrome
- Sox2 Anophthalmia Syndrome
- Sox2-Related Eye Disorders
- AEG Syndrome
- Anophthalmia, Clinical, With Associated Anomalies
- Anophthalmia-Esophageal-Genital Syndrome
- MCOPS3
- Syndromic Microphthalmia 3