| Human Disease |
Term: Microphthalmia, Syndromic 9; MCOPS9
OMIM ID: 601186
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| Synonyms |
Anophthalmia, Clinical, with Mild Facial Dysmorphism and Variable Malformations of the Lung, Heart, and Diaphragm; Anophthalmia/Microphthalmia and Pulmonary Hypoplasia; Matthew-Wood Syndrome; Spear Syndrome |
| Associated Genes |
Orthologous mouse and human markers where mutations in one or both species have been associated with phenotypes characteristic of this disease.
Mouse Gene |
Human Gene |
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Characteristics of this human disease are associated with mutations in... |
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 ...the human gene.
MGI data currently do not associate this disease with mutations in the orthologous mouse gene. |
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Analysis Tools