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ONTOLOGY REPORT - ANNOTATIONS


Term:Aland Island eye disease
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Accession:DOID:0050630 term browser browse the term
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. (DO)
Synonyms:exact_synonym: AIED;   Forsius-Eriksson syndrome;   Forsius-Eriksson type ocular albinism;   ocular albinism, type II
 primary_id: MESH:C562664
 alt_id: OMIM:300600;   RDO:0012280
 xref: GARD:10574
For additional species annotation, visit the Alliance of Genome Resources.


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Aland Island eye disease term browser
Symbol Object Name JBrowse Chr Start Stop Reference
G Cabp4 calcium binding protein 4 JBrowse link 1 219,383,452 219,388,009 RGD:8554872
G Cacna1f calcium voltage-gated channel subunit alpha1 F JBrowse link X 15,712,709 15,741,135 RGD:7240710
RGD:8554872
RGD:13782379
G Whrn whirlin JBrowse link 5 79,235,541 79,317,206 RGD:8554872

Term paths to the root
Path 1
Term Annotations click to browse term
  disease 15639
    sensory system disease 4697
      eye and adnexa disease 2257
        eye disease 2257
          Aland Island eye disease 3
Path 2
Term Annotations click to browse term
  disease 15639
    disease of anatomical entity 14969
      nervous system disease 10242
        sensory system disease 4697
          eye and adnexa disease 2257
            eye disease 2257
              Hereditary Eye Diseases 505
                Albinism 48
                  ocular albinism 8
                    Aland Island eye disease 3
paths to the root

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RGD is funded by grant HL64541 from the National Heart, Lung, and Blood Institute on behalf of the NIH.