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| Term | anterior segment dysgenesis 8 | ID (Ontology) | DOID:0080613 (Human Disease) |
| Definition | An anterior segment dysgenesis that has_material_basis_in homozygous or compound heterozygous mutation in the CPAMD8 gene on chromosome 19p13. | ||
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| DO.org | |||
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Full annotation statements including this term (annotations to child terms are NOT included), and relevant FlyBase records
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monogenic disease |__anterior segment dysgenesis__ autosomal genetic disease | |__autosomal recessive disease__| eye disease | |__anterior segment dysgenesis__| anterior segment dysgenesis 8 3 rec. |
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| Is a |
autosomal recessive disease anterior segment dysgenesis |
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External Crossreferences & Linkouts
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| MIM:617319 | |||