MeSH Browser

MeSH Supplementary: Microphthalmia, Syndromic 3
Unique ID: C565948
RDF Unique Identifier: http://id.nlm.nih.gov/mesh/C565948
Entry Term(s): AEG Syndrome; Anophthalmia, Clinical, With Associated Anomalies; Anophthalmia-Esophageal-Genital Syndrome; MCOPS3; Microphthalmia And Esophageal Atresia Syndrome; Sox2 Anophthalmia Syndrome; Sox2-Related Eye Disorders; Syndromic Microphthalmia 3
Registry Number: 0
Heading Mapped to: *Esophageal Atresia; *Microphthalmos; *Nervous System Malformations
Frequency: 7
Note: PROM mutation in SOX2
Date of Entry: 2012/11/05
Revision Date: 2013/10/24

Microphthalmia, Syndromic 3 MeSH Supplementary Concept Data 2024