OBO ID: DOID:0060839 |
Term Name: | isolated microphthalmia 2 | Search Ontology: | |
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Definition: | An isolated microphthalmia characterized by autosomal recessive inheritance of bilateral profound microphthalmia without associated anomalies and with normal intelligence that has_material_basis_in homozygous mutation in the CHX10 gene on chromosome 14q24. (2) | ||
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Ontology: | Human Disease ( DOID:0060839 ) |
OTHER isolated microphthalmia 2 PAGES
ZEBRAFISH MODELS
No data available
PHENOTYPE
No data available
CITATIONS: None
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