FB2025_05 , released December 11, 2025
FB2025_05 , released December 11, 2025
CV Term Report
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General Information
Term Aland Island eye disease ID (Ontology) DOID:0050630 (Human Disease)
Definition An eye disease characterized by fundus hypopigmentation, decreased visual acuity, nystagmus, astigmatism, myopia and defective darkness adaptation and has_material_basis_in mutation in the CACNA1F gene.
Also Known As "Forsius-Eriksson syndrome" ; "FORSIUS-ERIKSSON TYPE OCULAR ALBINISM"
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 Genes
 Aland Island eye disease       1
 for disease ribbon | Aland Island eye disease       1
 model of | Aland Island eye disease       1
Spanning Tree (Parents/Children)
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sensory system disease
 |__eye disease_________________
X-linked monogenic disease      |
 |__X-linked recessive disease__|
                                Aland Island eye disease  1 rec.
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Is a X-linked recessive disease
eye disease
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Synonyms
  • "Forsius-Eriksson syndrome" EXACT
    "FORSIUS-ERIKSSON TYPE OCULAR ALBINISM" EXACT
Secondary IDs
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GARD:10574
MESH:C562664
MIM:300600