• ABCA4 related disorders, MIM#601691
• PHARC Syndrome, MIM#612674
• Cone-rod dystropht 9, MIM#612775
• Weill-Marchesani syndrome 1, recessive
• Weill-Marchesani-like syndrome- lenticular myopia, ectopia lentis, glaucoma, spherophakia, and short stature, but no brachydactyly (AR)
• Usher Syndrome type 2C, MIM#605472
• Joubert Syndrome 3, MIM#608629
• AIPL1 related disorders, MIM#604392
• Alstrom syndrome, MIM#203800
• Joubert Syndrome 8, MIM#612291
• ARL6 related disorders, MIM#608845
• Glaucoma 1, open angle, F, MIM#603383
• AR Persistent hyperplasia of primary vitreous - optic nerve dysplasia, retinal detachment
• Bardet-Biedl syndrome 1 OMIM:209900;Bardet-Biedl syndrome 1 MONDO:0008854
• Bardet Biedl syndrome 10, 615987
• Bardet Biedl syndrome 12, 615989
• Bardet-Biedl syndrome 2, 615981
• Bardet-Biedl syndrome 4, 615982
• Bardet Biedl syndrome 5, 615983
• Bardet-Biedl syndrome 7, 615984
• Bardet Biedl syndrome 9, 615986
• Bardet-Biedl syndrome 21, OMIM:617406, MONDO:0044308;Cone-rod dystrophy 16, OMIM:614500, MONDO:0013786;Retinitis pigmentosa 64, OMIM:614500, MONDO:0019200
• Retinitis pigmentosa 49, OMIM:613756
• Glaucoma;anterior segment dysgenesis 8, 617319;retinal detachment;cataract
• Rubinstein-Taybi syndrome 1, OMIM:180849
• Glaucoma 3A, primary open angle, congenital, juvenile, or adult onset; 231300; Peters anomaly, 604229; Primary Congenital Glaucoma; Glaucoma 3, Primary Congenital, A; GLC3A;primary congenital glaucoma
• Singleton-Merten syndrome 2, OMIM:616298;Singleton-Merten syndrome 2, MONDO:0014575
• Retinitis pigmentosa 59, OMIM:613861
• Axenfeld-Rieger syndrome, type 3 602482;Anterior segment dysgenesis 3, multiple subtypes 601631
• Anterior segment dysgenesis;Peters anomaly;aniridia
• Anterior segment dysgenesis 2, multiple subtypes 610256
• Oculodentodigital dysplasia, OMIM:164200
• Singleton-Merten syndrome 1, OMIM:182250
• Bardet-Biedl syndrome 19, 615996
• Bardet-Biedl syndrome 20, 617119
• Nail-patella syndrome, OMIM:161200
• Primary Congenital Glaucoma;Glaucoma 3, primary congenital, D 613086
• Bardet-Biedl syndrome 17, 615994
• Bardet-Biedl syndrome 6, 605231;McKusick-Kaufman syndrome, 236700
• Bardet-Biedl syndrome 13, 615990;Meckel syndrome 1, 249000;Joubert syndrome 28, 617121
• Glaucoma 1A, primary open angle, 137750
• Glaucoma 1, open angle, 1O, 613100
• Lowe syndrome, OMIM:309000
• Glaucoma 1, open angle, E, OMIM:137760;{Glaucoma, normal tension, susceptibility to}, OMIM:606657;Adult-onset
• PAX6 related disorders, MIM#607108
• Anterior segment dysgenesis 4 137600;Axenfeld-Rieger syndrome, type 1 180500
• Charcot-Marie-Tooth disease, type 4B2, OMIM:604563;CMT with early onset glaucoma
• Frank-ter Haar syndrome, OMIM:249420
• Primary Angle Closure Glaucoma
• Glaucoma 3, primary congenital, E, OMIM:617272
• Bardet-Biedl syndrome 8, 615985
• Glaucoma 1, open angle, G 609887