Phenotypes for disease #00293 (FVH2 (hypoplasia, foveal, type 2, with or without optic nerve misrouting and/or anterior segment dysgenesis), OMIM:609218)

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0000002899 secondary nystagmus and low vision - FVH2 Familial, autosomal recessive - - - - - Yonatan Perez 00001640
0000128051 - Foveal hypoplasia - Familial, autosomal recessive - - - - - Dror Sharon 00155551
0000292447 Hypoplasia of the fovea (HP:0007750), reduced visual acuity (HP:0007663), nystagmus (HP:0000639) and optic nerve misrouting (HP:0025551). Idiopathic infantile nystagmus Foveal Hypoplasia 2 Familial, autosomal recessive - 06y - - - Mohammed A.M Derar 00399330
0000292467 Hypoplasia of the fovea (HP:0007750), reduced visual acuity (HP:0007663), nystagmus (HP:0000639) and optic nerve misrouting (HP:0025551) PAX6 related phenotype Foveal Hypoplasia 2 Familial, autosomal recessive - 10y - - - Mohammed A.M Derar 00399350
0000292468 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 - 18y - - rs1161159416 Mohammed A.M Derar 00399351
0000292470 secondary nystagmus and low vision - FVH2 Familial, autosomal recessive - - - - - Yonatan Perez 00399353
0000292471 secondary nystagmus and low vision - FVH2 Familial, autosomal recessive - - - - - Yonatan Perez 00399354
0000292472 see paper; ..., foveal hypoplasia, optic nerve misrouting, Kartagener syndrome foveal hypoplasia, Kartagener syndrome FVH2 Familial, autosomal recessive - - - - - Johan den Dunnen 00399357
0000292473 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 - 18y - - rs1161159416 Mohammed A.M Derar 00399362
0000292474 foveal hypoplasia (HP:0007750), reduced visual acuity (HP:0007663), nystagmus (HP:0000639), optic nerve misrouting (HP:0025551) - FVH2 Familial, autosomal recessive - - - - - Johan den Dunnen 00399363
0000292475 foveal hypoplasia (HP:0007750), nystagmus (HP:0000639) - FVH2 Familial, autosomal recessive - - - - - Johan den Dunnen 00399364
0000292476 foveal hypoplasia (HP:0007750), nystagmus (HP:0000639) - FVH2 Familial, autosomal recessive - - - - - Johan den Dunnen 00399365
0000292477 foveal hypoplasia (HP:0007750), nystagmus (HP:0000639) - FVH2 Familial, autosomal recessive - - - - - Johan den Dunnen 00399366
0000292492 ypoplasia of the fovea (HP:0007750), reduced visual acuity (HP:0007663), nystagmus (HP:0000639), optic nerve misrouting (HP:0025551), posterior embryotoxon (HP:0000627) and Hypopigmentation of the fundus (HP:0007894) ocular albinism Foveal hypoplasia 2 Familial, autosomal recessive - 14y - - - Mohammed A.M Derar 00399380
0000292498 Hypoplasia of the fovea (HP:0007750), reduced visual acuity (HP:0007663), nystagmus (HP:0000639), astigmatism (HP:0000483) and moderate hypermetropia (HP:0031729) Albinism Foveal Hypoplasia Familial, autosomal recessive - 32y - - - Mohammed A.M Derar 00399387
0000292505 Hypoplasia of the fovea (HP:0007750), reduced visual acuity (HP:0007663) and nystagmus (HP:0000639). - - Familial, autosomal recessive - 02y - - - Mohammed A.M Derar 00399394
0000292518 Hypoplasia of the fovea (HP:0007750), Nystagmus (HP:0000639), Hypopigmentation of the fundus (HP:0007894), Posterior embryotoxon (HP:0000627), Reduced visual acuity (HP:0007663) and Optic nerve misrouting (HP:0025551) - Foveal hypoplasia 2 Familial, autosomal recessive - 74y - - - Mohammed A.M Derar 00399407
0000292519 Hypoplasia of the fovea (HP:0007750), Nystagmus (HP:0000639) and Iris transillumination defect (HP:0012805) Albinism Foveal hypoplasia 2 Familial, autosomal recessive - - - - rs1161159416 Mohammed A.M Derar 00399408
0000292521 Hypoplasia of the fovea (HP:0007750), Nystagmus (HP:0000639), Hypermetropia (HP:0000540) and Astigmatism (HP:0000483) - - Unknown - - - - - Mohammed A.M Derar 00399411
0000292573 ypoplasia of the fovea (HP:0007750), Nystagmus (HP:0000639),Hypermetropia (HP:0000540) and Astigmatism (HP:0000483) - - Familial, autosomal recessive - - - - - Mohammed A.M Derar 00399468
0000292574 Hypoplasia of the fovea (HP:0007750), Nystagmus (HP:0000639),Hypermetropia (HP:0000540), Astigmatism (HP:0000483), Reduced visual acuity (HP:0007663), Strabismus (HP:0000486) and Iris transillumination defect (HP:0012805) - - Familial, autosomal recessive - - - - - Mohammed A.M Derar 00399470
0000292577 Hypoplasia of the fovea (HP:0007750) and Reduced visual acuity (HP:0007663) - - Familial, autosomal recessive - - - - - Mohammed A.M Derar 00399472
0000292619 Hypoplasia of the fovea (HP:0007750), reduced visual acuity (HP:0007663), nystagmus (HP:0000639) and strabismus (HP:0000486) - Foveal Hypoplasia 2 Familial, autosomal recessive - 03y - - - Mohammed A.M Derar 00399514
0000292620 Hypoplasia of the fovea (HP:0007750), reduced visual acuity (HP:0007663), nystagmus (HP:0000639), optic nerve misrouting (HP:0025551), posterior embryotoxon (HP:0000627) and strabismus (HP:0000486) - Foveal Hypoplasia 2 Familial, autosomal recessive - 16y - - - Mohammed A.M Derar 00399515
0000292621 Hypoplasia of the fovea (HP:0007750), reduced visual acuity (HP:0007663), nystagmus (HP:0000639) & strabismus (HP:0000486) - Foveal Hypoplasia 2 Familial, autosomal recessive - 21y - - - Mohammed A.M Derar 00399516
0000292623 Hypoplasia of the fovea (HP:0007750), reduced visual acuity (HP:0007663), nystagmus (HP:0000639), optic nerve misrouting (HP:0025551), posterior embryotoxon (HP:0000627) and cataracts (HP:0000518) - Foveal Hypoplasia 2 Familial, autosomal recessive - 39y - - - Mohammed A.M Derar 00399518
0000292640 Hypoplasia of the fovea (HP:0007750), reduced visual acuity (HP:0007663), nystagmus (HP:0000639), optic nerve misrouting (HP:0025551) and (HP:0012805) and strabismus (HP:0000486). - Foveal Hypoplasia 2 Familial, autosomal recessive - 05y - - - Mohammed A.M Derar 00399535
0000292641 Hypoplasia of the fovea (HP:0007750), reduced visual acuity (HP:0007663), nystagmus (HP:0000639), optic nerve misrouting (HP:0025551), Shallow anterior chamber (HP:0000594) and strabismus (HP:0000486) - Foveal Hypoplasia 2 Familial, autosomal recessive - 36y - - - Mohammed A.M Derar 00399536
0000292642 Hypoplasia of the fovea (HP:0007750), reduced visual acuity (HP:0007663), nystagmus (HP:0000639) and strabismus (HP:0000486). - Foveal Hypoplasia 2 Familial, autosomal recessive - 05y - - - Mohammed A.M Derar 00399537
0000292643 Hypoplasia of the fovea (HP:0007750), reduced visual acuity (HP:0007663), nystagmus (HP:0000639),strabismus (HP:0000486) and infantile nystagmus and foveal hypoplasia Foveal Hypoplasia 2 Familial, autosomal recessive - 40y - - ummmamd@leeds.ac.uk Mohammed A.M Derar 00399538
0000292646 Hypoplasia of the fovea (HP:0007750), Nystagmus (HP:0000639), Reduced visual acuity (HP:0007663) and strabismus (HP:0000486). infantile nystagmus and foveal hypoplasia Foveal Hypoplasia 2 Familial, autosomal recessive - 03y - - - Mohammed A.M Derar 00399541
0000293096 Hypoplasia of the fovea (HP:0007750), reduced visual acuity (HP:0007663), nystagmus (HP:0000639) and strabismus (HP:0000486). - Foveal Hypoplasia 2 Familial, autosomal recessive - 03y - - - Mohammed A.M Derar 00400055
0000293097 see paper; ... - - Familial, autosomal recessive - - - - - Johan den Dunnen 00400056
0000293112 see paper; ... - - Familial, autosomal recessive - - - - - Johan den Dunnen 00400071
0000293113 see paper; ... - - Familial, autosomal recessive - - - - - Johan den Dunnen 00400072
0000293114 Hypoplasia of the fovea (HP:0007750), reduced visual acuity (HP:0007663), nystagmus (HP:0000639) and macrocephaly (HP:0000256) - Foveal Hypoplasia 2 Familial, autosomal recessive - 01y - - - Mohammed A.M Derar 00400073
0000293115 Hypoplasia of the fovea (HP:0007750), reduced visual acuity (HP:0007663), strabismus (HP:0000486) and nystagmus (HP:0000639) - Foveal Hypoplasia 2 Familial, autosomal recessive - 01y - - - Mohammed A.M Derar 00400074
0000293126 Hypoplasia of the fovea (HP:0007750), reduced visual acuity (HP:0007663) and nystagmus (HP:0000639). - Foveal Hypoplasia 2 Familial, autosomal recessive - 02y - - - Mohammed A.M Derar 00400085
0000294216 see paper; ... - FVH2 Familial, autosomal recessive - 02y - - - Johan den Dunnen 00401173
0000294421 Hypoplasia of the fovea (HP:0007750), reduced visual acuity (HP:0007663), nystagmus (HP:0000639) and optic nerve misrouting (HP:0025551) - Foveal hypoplasia 2 Familial, autosomal recessive - - - - - Mohammed A.M Derar 00401649
0000294424 Hypoplasia of the fovea (HP:0007750), reduced visual acuity (HP:0007663), nystagmus (HP:0000639), optic nerve misrouting (HP:0025551) - Foveal Hypoplasia Familial, autosomal recessive - - - - - Mohammed A.M Derar 00401650
0000294425 Hypoplasia of the fovea (HP:0007750), reduced visual acuity (HP:0007663) and nystagmus (HP:0000639), - Foveal Hypoplasia 2 Familial, autosomal recessive - - - - - Mohammed A.M Derar 00401651
0000295071 Hypoplasia of the fovea (HP:0007750), reduced visual acuity (HP:0007663), nystagmus (HP:0000639) and strabismus (HP:0000486). - Foveal Hypoplasia 2 Familial, autosomal recessive - 28y - - - Mohammed A.M Derar 00402309
0000295072 Hypoplasia of the fovea (HP:0007750), reduced visual acuity (HP:0007663), nystagmus (HP:0000639) and strabismus (HP:0000486). - Foveal Hypoplasia 2 Familial, autosomal recessive - 19y - - - Mohammed A.M Derar 00402310
0000295074 Hypoplasia of the fovea (HP:0007750), reduced visual acuity (HP:0007663), nystagmus (HP:0000639) and strabismus (HP:0000486). - Foveal Hypoplasia 2 Familial, autosomal recessive - 12y - - - Mohammed A.M Derar 00402312
0000295075 Hypoplasia of the fovea (HP:0007750), reduced visual acuity (HP:0007663), nystagmus (HP:0000639) and strabismus (HP:0000486). - Foveal Hypoplasia 2 Familial, autosomal recessive - 08y - - - Mohammed A.M Derar 00402313
0000295077 Hypoplasia of the fovea (HP:0007750), reduced visual acuity (HP:0007663) and nystagmus (HP:0000639) - Foveal Hypoplasia 2 Familial, autosomal recessive - 01y - - - Mohammed A.M Derar 00402315
0000295079 Hypoplasia of the fovea (HP:0007750), reduced visual acuity (HP:0007663) and nystagmus (HP:0000639) - Foveal Hypoplasia 2 Familial, autosomal recessive - 06y - - - Mohammed A.M Derar 00402317
0000295080 Hypoplasia of the fovea (HP:0007750), reduced visual acuity (HP:0007663), nystagmus (HP:0000639) and posterior embryotoxon (HP:0000627) - Foveal Hypoplasia 2 Familial, autosomal recessive - 50y - - - Mohammed A.M Derar 00402318
0000295103 Hypoplasia of the fovea (HP:0007750), reduced visual acuity (HP:0007663), nystagmus (HP:0000639), optic nerve misrouting (HP:0025551), iris transillumination defect (HP:0012805) and strabismus (HP:0000486) - Foveal Hypoplasia 2 Familial, autosomal recessive - 16y - - - Mohammed A.M Derar 00402341
0000295112 Hypoplasia of the fovea (HP:0007750), reduced visual acuity (HP:0007663), nystagmus (HP:0000639), optic nerve misrouting (HP:0025551) and (HP:0012805) and strabismus (HP:0000486). - foveal hypoplasia 2 Familial, autosomal recessive - 13y - - - Mohammed A.M Derar 00402350
0000298473 Hypoplasia of the fovea (HP:0007750), reduced visual acuity (HP:0007663), nystagmus (HP:0000639), Posterior embryotoxon (HP:0000627) & goniodysgenesis. - Foveal Hypoplasia 2 Familial, autosomal recessive 03y - - - - Mohammed A.M Derar 00405975
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