Phenotype ID
Phenotype details
Diagnosis/Initial
Diagnosis/Definite
Inheritance
Age/Examination
Age/Diagnosis
Age/Onset
Phenotype/Onset
Protein
Owner
Individual ID
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