Phenotypes for disease #03946 (RP82 (retinitis pigmentosa, with/without situs inversus (RP82)), OMIM:615434)

5 entries on 1 page. Showing entries 1 - 5.
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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     
0000117813 HP:0007663, reduced visual acuity; HP:0000505, visual impairment; HP:0007722, retinal pigment epithelial atrophy; HP:0007843, attenuation of retinal blood vessels; HP:0007737; bone spicule pigmentation of the retina; HP:0001133, constriction of peripheral visual field; HP:0000662, nyctalopia - - Familial, autosomal recessive 41y 41y 16y - - Hao Deng 00145073
0000127224 ... - - Familial, autosomal recessive - - - - - Dror Sharon 00154483
0000132900 non-syndromic Retinitis pigmentosa simplex RP simplex RP Isolated (sporadic) 24y 24y 18y Night blindness - María González-del Pozo 00168037
0000132901 non-syndromic RP simplex RP simplex RP Unknown 25y - 25y Night blindness - María González-del Pozo 00168038
0000132902 non-syndromic RP simplex RP simplex RP Unknown 48y - 18y HP:0000662 - María González-del Pozo 00168039
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