Phenotypes for disease #04213 (COD (dystrophy, cone (COD)))

19 entries on 1 page. Showing entries 1 - 19.
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AscendingPhenotype ID     

Phenotype details     

Diagnosis/Initial     

Diagnosis/Definite     

Inheritance     

Age/Examination     

Age/Diagnosis     

Age/Onset     

Phenotype/Onset     

Protein     

Owner     

Individual ID     
0000026774 - - - Familial, autosomal recessive - - - - - Leen Abu Safieh 00033345
0000027066 - - - Familial, autosomal dominant - - - - - Marta de Castro-Miró 00033637
0000027103 - - - Isolated (sporadic) - - - - - Nathalie Bax 00033674
0000055854 cone dystrophy (HP:0000548); Reduced cone ERGs, normal rod ERGs, OD: 0.02, OS: 0.07 - - Familial, autosomal recessive - - 10y unknown - Stéphanie Cornelis 00076079
0000055855 cone dystrophy (HP:0000548); Reduced cone ERGs, normal rod ERGs, OD: 0.05, OS: 0.1 - - Familial, autosomal recessive - - 6y unknown - Stéphanie Cornelis 00076080
0000055863 cone dystrophy (HP:0000548); Reduced cone ERGs, normal rod ERGs, OD: 0.1, OS: 0.1, Central scotoma - - Familial, autosomal recessive - - 7y unknown - Stéphanie Cornelis 00076088
0000057894 cone dystrophy (HP:0000548) - - Unknown - - - unknown - Stéphanie Cornelis 00078119
0000057895 cone dystrophy (HP:0000548) - - Unknown - - - unknown - Stéphanie Cornelis 00078120
0000057896 cone dystrophy (HP:0000548) - - Unknown - - - unknown - Stéphanie Cornelis 00078121
0000057897 cone dystrophy (HP:0000548) - - Unknown - - - unknown - Stéphanie Cornelis 00078122
0000060677 cone dystrophy - - Unknown 05y - - - - Lonneke Haer-Wigman 00080792
0000067473 - - - Familial, autosomal recessive - - - - - Leen Abu Safieh 00087952
0000082882 - - - Familial, autosomal recessive - - - - - Marta de Castro-Miró 00104993
0000135710 - - - Familial, autosomal recessive - 05y 02y - - María González-del Pozo 00170849
0000243071 see paper; ..., decreased central vision (HP:0007663), extreme photophobia (HP:0000613), progressive visual loss in both eyes (HP:0000529), dyschromatopsia (HP:0007641), absent rod-and cone-mediated responses on ERG (HP:0007688) cone dystrophy - Familial, autosomal recessive - 20y 06y photophobia, reduiced visual acuity - Najlae Akhiyate 00324526
0000243094 - COD COD Familial, autosomal recessive 17y 17y 13y - - Qing Zhu 00324584
0000244574 photophobia (HP:0000613), reduced visual acuity (HP:0007663), paracentral scotoma (HP:0030528) cone dystrophy - Familial, autosomal recessive - - - photophobia (HP:0000613) - Jens Doets 00324522
0000245278 photophobia (HP:0000613), progressive visual loss in both eyes (HP:0000529), reduced visual acuity (HP:0007663), Dyschromatopsia (HP:0007641), Absent rod-and cone-mediated responses on ERG (HP:0007688) cone dystrophy - Familial, autosomal recessive 20y - - photophobia (HP:0000613) - Jens Doets 00326802
0000308986 see paper cone dystrophy - Unknown - - - - - Johan den Dunnen 00417505
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