Phenotypes for disease #02508 (LCA4 (Leber congenital amaurosis, type 4 (LCA4)), OMIM:604393)

11 entries on 1 page. Showing entries 1 - 11.
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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     
0000026820 Rdwith Md; Onset Nystagmus, No Keratoconus - - Familial, autosomal recessive 9y - - - - Raheel Qamar 00033391
0000026821 Rdwith Md; Onset Nystagmus, No Keratoconus - - Familial, autosomal recessive 13y - - - - Raheel Qamar 00033392
0000026878 Rdwith Md; Onset Nystagmus, No Keratoconus - - Familial, autosomal recessive 79y - - - - Raheel Qamar 00033449
0000026926 salt andpepper fundus; Onset Nystagmus, No Keratoconus - - Familial, autosomal recessive 5y - - - - Raheel Qamar 00033497
0000026973 Rdwith Md; Onset Nystagmus, No Keratoconus - - Familial, autosomal recessive 10y - - - - Raheel Qamar 00033544
0000026974 Rdwith Md; Onset Nystagmus, No Keratoconus - - Familial, autosomal recessive 19y - - - - Raheel Qamar 00033545
0000026975 Rdwith Md; Onset Right Eye Keratoconus - - Familial, autosomal recessive 3y - - - - Raheel Qamar 00033546
0000026976 Rdwith Md; Onset Right Eye Keratoconus - - Familial, autosomal recessive 37y - - - - Raheel Qamar 00033547
0000026977 Rdwith Md; Onset Nystagmus, No Keratoconus - - Familial, autosomal recessive 44y - - - - Raheel Qamar 00033548
0000026996 Rdwith Md; Onset Right Eye Keratoconus - - Familial, autosomal recessive 41y - - - - Raheel Qamar 00033567
0000060594 Leber congenital amaurosis 4 (OMIM:604393) - - Familial, autosomal recessive - - - - - Daniel Trujillano 00081025
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