Phenotypes for disease #01335 (FVH1 (Foveal hypoplasia 1), OMIM:136520)

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AscendingPhenotype ID     

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Individual ID     
0000292446 Hypoplasia of the fovea (HP:0007750), reduced visual acuity (HP:0007663), nystagmus (HP:0000639), optic nerve misrouting (HP:0025551) and strabismus (HP:0000486) PAX6 related phenotype Foveal Hypoplasia 2 Familial, autosomal recessive - 27y - - rs1161159416 Mohammed A.M Derar 00399329
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