OBO ID: DOID:0060842 |
Term Name: | isolated microphthalmia 3 | Search Ontology: | |
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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) | ||
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Ontology: | Human Disease ( DOID:0060842 ) |
OTHER isolated microphthalmia 3 PAGES
ZEBRAFISH MODELS
No data available
PHENOTYPE
No data available
CITATIONS: None
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