Disease #01425 (ARMD2 (macular degeneration, age-related, type 2 (ARMD-2)), OMIM:153800)

Official abbreviation ARMD2
Name macular degeneration, age-related, type 2 (ARMD-2)
OMIM ID 153800
Human Phenotype Ontology Project (HPO) HPO
Inheritance Autosomal dominant
Individuals reported having this disease 1
Phenotype entries for this disease 1
Associated with 1 gene ABCA4
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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00080786 - - - ? no - - - - - - ARMD2 - - ABCA4 2 1 Lonneke Haer-Wigman
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