|OBO ID: DOID:0060842|
|Term Name:||isolated microphthalmia 3||Search Ontology:|
|Definition:||An isolated microphthalmia characterized by clinical anophthalmia and/or microphthalmia that has_material_basis_in compound heterozygous mutation in the RAX gene on chromosome 18q21. (2)|
|Ontology:||Human Disease (DOID:0060842)|
|is a type of:||
OTHER isolated microphthalmia 3 PAGES
ZEBRAFISH MODELS No data available
PHENOTYPE No data available
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