Phenotypes for disease #04618 (CORD20 (dystrophy, cone-rod, type 20 (CORD20)), OMIM:615973)

2 entries on 1 page. Showing entries 1 - 2.
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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     
0000243075 decreased central vision (HP:0007663), dyschromatopsia (HP:0000551) and extreme photophobia (HP:0000613) cone-rod dystrophy CORD20 Familial, autosomal recessive 61y - - - - Najlae Akhiyate 00324548
0000267011 (+) Visual impairment,(+) Cone/cone-rod dystrophy/ Cone-rod dystrophy, onset at about 12 years, now visual acuity at 10%, parents consanguine (cosuins 1°) - 14y Unknown - - 12y - - Andreas Laner 00371675
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