Phenotypes for disease #02467 (STGD4 (Stargardt disease, type 4 (STGD-4)), OMIM:603786)

4 entries on 1 page. Showing entries 1 - 4.
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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     
0000026255 macular degeneration - - Unknown - - - - - Pascal Escher 00032826
0000326642 Photophobia HP:0000613, Reduced visual acuity HP:0007663, Large central visual field defect HP:0001129, Color vision defect HP: 0000551, Central scotoma HP: 0000603, Abnormality of macular pigmentation HP: 0008002 Stargardt STGD4 Familial, autosomal recessive 10y 22y 05y - - Rocio Villafuerte-de la Cruz 00436465
0000326650 Photophobia HP:0000613, Reduced visual acuity HP:0007663, Large central visual field defect HP:0001129, Color vision defect HP: 0000551, Central scotoma HP: 0000603, Abnormality of macular pigmentation HP: 0008002 Stargardt STGD4 Familial, autosomal recessive 38y 38y 23y 23y - Rocio Villafuerte-de la Cruz 00436472
0000326652 Photophobia HP:0000613, Reduced visual acuity HP:0007663, Large central visual field defect HP:0001129, Color vision defect HP: 0000551, Central scotoma HP: 0000603, Abnormality of macular pigmentation HP: 0008002 Stargardt STGD4 Familial, autosomal recessive 28y 28y 08y 8y - Rocio Villafuerte-de la Cruz 00436474
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