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

Official abbreviation STGD4
Name Stargardt disease, type 4 (STGD-4)
OMIM ID 603786
Human Phenotype Ontology Project (HPO) HPO
Inheritance Autosomal dominant
Individuals reported having this disease 4
Phenotype entries for this disease 4
Associated with 1 gene PROM1
Associated tissues -
Disease features -
Remarks -
Date created 2014-09-25 23:29:40 +02:00 (CEST)
Date last edited 2021-12-10 21:51:32 +01:00 (CET)


Individuals

4 entries on 1 page. Showing entries 1 - 4.
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00032826 - PubMed: Kniazeva 1999 - - - - Caribbean - - - - STGD4 macular degeneration PROM1 PROM1 1 23 Pascal Escher
00436465 2324887 Villafuerte-de la Cruz RA, et al., 2023. Submitted - M no (Mexico) Hispanic - - - none STGD4 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 PROM1 PROM1 2 1 Rocio Villafuerte-de la Cruz
00436472 2694968 Villafuerte-de la Cruz RA, et al., 2023. Submitted - F no Mexico Hispanic - - - none STGD4 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 PROM1 PROM1 2 1 Rocio Villafuerte-de la Cruz
00436474 2696196 Villafuerte-de la Cruz RA, et al., 2023. Submitted - F no Mexico Hispanic - - - none STGD4 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 PROM1 PROM1 1 1 Rocio Villafuerte-de la Cruz
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