Search Ontology:
Human Disease
syndromic microphthalmia 3
- Term ID
- DOID:0111801
- Synonyms
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- AEG syndrome
- anophthalmia clinical with associated anomalies
- anophthalmia esophageal genital syndrome
- anophthalmia microphthalmia esophageal atresia
- anophthalmia/microphthalmia-esophageal atresia syndrome
- MCOPS3
- microphthalmia and esophageal atresia syndrome
- SOX2 anophthalmia syndrome
- syndromic microphthalmia type 3
- Definition
- A syndromic microphthalmia characterized by clinical anophthalmia or microphthalmia, with various extraocular symptoms that has_material_basis_in heterozygous mutation in the SOX2 gene on chromosome 3q26.33. (2)
- References
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- GARD:1443
- MESH:C565948
- MIM:206900
- ORDO:77298
- SNOMEDCT_US_2023_03_01:698851003
- UMLS_CUI:C1859773
- Ontology
- Human Disease ( DOID:0111801 )
- is a type of
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Genes Involved
Zebrafish Models