FB2025_05 , released December 11, 2025
FB2025_05 , released December 11, 2025
CV Term Report
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General Information
Term isolated microphthalmia 8 ID (Ontology) DOID:0060841 (Human Disease)
Definition An isolated microphthalmia characterized by bilateral severe microphthalmia autosomal recessive inheritance of that has_material_basis_in homozygous mutation in the ALDH1A3 gene on chromosome 15q26.
Also Known As "MCOP8"
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 Genes
 isolated microphthalmia 8       2
 for disease ribbon | isolated microphthalmia 8       2
 model of | isolated microphthalmia 8       2
Spanning Tree (Parents/Children)
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autosomal genetic disease
 |__autosomal recessive disease__
microphthalmia                   |
 |__isolated microphthalmia______|
                                 isolated microphthalmia 8  2 rec.
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Is a autosomal recessive disease
isolated microphthalmia
Part of
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Synonyms
  • "MCOP8" EXACT OMO:0003012
Secondary IDs
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ICD10CM:Q11.0
MIM:615113
ORDO:2542