Phenotypes for disease #01507 (PPCRA (atrophy, chorioretinal, pigmented paravenous (PPCRA)), OMIM:172870)

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     
0000028467 Presence of bilaterally symmetrical chorioretinal atrophy, with accumulation of bone corpuscle pigmentation along the retinal veins - - Familial, autosomal dominant - - - ? - Frans Cremers 00037924
0000028468 Presence of bilaterally symmetrical chorioretinal atrophy, with accumulation of bone corpuscle pigmentation along the retinal veins - - Familial, autosomal dominant - - - ? - Frans Cremers 00037925
0000028469 Presence of bilaterally symmetrical chorioretinal atrophy, with accumulation of bone corpuscle pigmentation along the retinal veins - - Familial, autosomal dominant - - - ? - Frans Cremers 00037926
0000028470 Presence of bilaterally symmetrical chorioretinal atrophy, with accumulation of bone corpuscle pigmentation along the retinal veins - - Familial, autosomal dominant - - - ? - Frans Cremers 00037927
0000028471 Presence of bilaterally symmetrical chorioretinal atrophy, with accumulation of bone corpuscle pigmentation along the retinal veins - - Familial, autosomal dominant - - - ? - Frans Cremers 00037928
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