Phenotypes for disease #00485 (OA1 (albinism, ocular, type I (OA-1,Nettleship-Falls type)), OMIM:300500)

7 entries on 1 page. Showing entries 1 - 7.
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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     
0000060795 no cutaneous involvement - - Familial, X-linked - - - - - Gemeinschaftspraxis für Humangenetik Dresden 00080700
0000082910 - - - Familial, autosomal dominant - - - - - Marta de Castro-Miró 00105018
0000278037 - optical atrophy - Familial, X-linked - - - - - LOVD 00384252
0000278052 - optical atrophy - Familial, X-linked - - - - - LOVD 00384267
0000278083 - optical atrophy - Familial, X-linked - - - - - LOVD 00384298
0000278183 - Ocular albinism - Familial, X-linked - - - - - LOVD 00384398
0000278200 - optical atrophy - Familial, X-linked - - - - - LOVD 00384415
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