Phenotypes for disease #00421 (CORD3 (dystrophy, cone rod, type 3 (CORD-3)), OMIM:604116)

13 entries on 1 page. Showing entries 1 - 13.
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Phenotype details     

Diagnosis/Initial     

Diagnosis/Definite     

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Age/Examination     

Age/Diagnosis     

Age/Onset     

Phenotype/Onset     

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Owner     

Individual ID     
0000054431 Stargardt disease; Visual acuity: OD 20/400, OS 20/400, Resorption of flecks. Choriocapillaris atrophy within the macula was often observed in these patients.. - - Unknown - - - - - Stéphanie Cornelis 00016875
0000054441 cone-rod dystrophy (HP:0000510); Visual acuity: OD count fingers, OS count fingers, Resorption of flecks. Choriocapillaris atrophy within the macula was often observed in these patients.. - - Unknown - - - - - Stéphanie Cornelis 00016897
0000054444 cone-rod dystrophy (HP:0000510); Visual acuity: OD count fingers, OS count fingers, Resorption of flecks. Choriocapillaris atrophy within the macula was often observed in these patients.. - - Unknown - - - - - Stéphanie Cornelis 00016900
0000054452 - - - Unknown - - - - - Stéphanie Cornelis 00016909
0000054458 cone-rod dystrophy (HP:0000510); Visual acuity: OD 5/180+1, OS 5/160+1. - - Unknown - - - - - Stéphanie Cornelis 00016917
0000243063 - CORD CORD3 Familial, autosomal recessive 38y 38y 13y - - Qing Zhu 00324520
0000243087 - CORD CORD3 Familial, autosomal recessive 33y 33y 20y - - Qing Zhu 00324560
0000243088 - CORD CORD3 Familial, autosomal recessive 07y 07y 05y - - Qing Zhu 00324561
0000243089 - CORD CORD3 Familial, autosomal recessive 27y 27y 17y - - Qing Zhu 00324562
0000243090 - CORD CORD3 Familial, autosomal recessive 18y 18y 12y - - Qing Zhu 00324579
0000243091 - CORD CORD3 Familial, autosomal recessive 10y 10y 09y - - Qing Zhu 00324580
0000243093 - CORD CORD3 Familial, autosomal recessive 20y 20y 10y - - Qing Zhu 00324582
0000300906 - - (CORD-3) Familial, autosomal recessive - - - - - Nancy Xilotl de Jesús 00408788
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