Disease #01696 (ODRMD (optic disc anomalies with retinal and/or macular dystrophy (ODRMD)), OMIM:212550)

Official abbreviation ODRMD
Name optic disc anomalies with retinal and/or macular dystrophy (ODRMD)
OMIM ID 212550
Human Phenotype Ontology Project (HPO) HPO
Inheritance Autosomal recessive
Individuals reported having this disease 1
Phenotype entries for this disease 1
Associated with 1 gene SIX6
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

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00409553 K6671 PubMed: Oishi 2018 - F - Japan - - - - - ODRMD best corrected visual acuity: 1.2; electroretinogram , rod: mildly reduced, cone: mildly reduced CYP4V2 CYP4V2 1 1 LOVD
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