FB2025_05 , released December 11, 2025
FB2025_05 , released December 11, 2025
CV Term Report
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General Information
Term anterior segment dysgenesis 7 ID (Ontology) DOID:0080612 (Human Disease)
Definition An anterior segment dysgenesis that has_material_basis_in homozygous or compound heterozygous mutation in the PXDN gene on chromosome 2p25.
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 Genes
 anterior segment dysgenesis 7       7
 for disease ribbon | anterior segment dysgenesis 7       7
 model of | anterior segment dysgenesis 7       7
Spanning Tree (Parents/Children)
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monogenic disease
 |__anterior segment dysgenesis__
autosomal genetic disease        |
 |__autosomal recessive disease__|
eye disease                      |
 |__anterior segment dysgenesis__|
                                 anterior segment dysgenesis 7  7 rec.
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Is a autosomal recessive disease
anterior segment dysgenesis
Part of
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MIM:269400