Phenotypes for disease #03440 (RP40 (retinitis pigmentosa, type 40 (RP40)), OMIM:613801)

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     
0000275979 retinal dystrophy; MIM, 613801 or 163500 MIM, 613801 or 163500 - Familial, autosomal recessive - - - - - LOVD 00382137
0000304647 Retinitis pigmentosa Retinal dystrophy Retinitis pigmentosa Familial, autosomal recessive - - - - khadim Khadim Shah 00412655
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