Phenotypes for disease #02286 (RP12 (retinitis pigmentosa, with/without PPRPE, type 12), OMIM:600105)

12 entries on 1 page. Showing entries 1 - 12.
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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     
0000028455 Night blindness, loss of peripheral vision, strabismus - - Familial, autosomal recessive - - - ? - Frans Cremers 00037912
0000028456 Night blindness, loss of peripheral vision, strabismus - - Familial, autosomal recessive - - - ? - Frans Cremers 00037913
0000028457 Night blindness, loss of peripheral vision, strabismus - - Familial, autosomal recessive - - - ? - Frans Cremers 00037914
0000028458 Night blindness, loss of peripheral vision, strabismus - - Familial, autosomal recessive - - - ? - Frans Cremers 00037915
0000028459 Night blindness, loss of peripheral vision, strabismus - - Familial, autosomal recessive - - - ? - Frans Cremers 00037916
0000028460 Night blindness, loss of peripheral vision, strabismus - - Unknown - - - ? - Frans Cremers 00037917
0000028461 Night blindness, loss of peripheral vision, strabismus - - Familial, autosomal recessive - - - ? - Frans Cremers 00037918
0000028462 Night blindness, loss of peripheral vision, strabismus - - Familial, autosomal recessive - - - ? - Frans Cremers 00037919
0000028463 Night blindness, loss of peripheral vision, strabismus - - Familial, autosomal recessive - - - ? - Frans Cremers 00037920
0000028464 Night blindness, loss of peripheral vision, strabismus - - Unknown - - - ? - Frans Cremers 00037921
0000028484 ? - - Familial, autosomal recessive - - - ? - Frans Cremers 00037941
0000275975 retinal dystrophy; MIM, 600105, 613835 MIM, 600105, 613835 - Familial, autosomal recessive - - - - - LOVD 00382133
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