Phenotypes for disease #00702 (LCA10 (Leber congenital amaurosis, type 10 (LCA-10)), OMIM:611755)

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     
0000326753 Blindness HP:0000618, Retinitis pigmentosa HP:0000510 - # 611755 Familial, autosomal recessive 01y 04y 00y04m - - Rocio Villafuerte-de la Cruz 00436606
0000326850 HP: 0007875 Congenital Amaurosis LCA10 # 611755 Familial, autosomal recessive 00y04m 04y 00y04m 0y04m - Rocio Villafuerte-de la Cruz 00436736
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