Disease #05876 (RDMS (dystrophy, retinal, with macular staphyloma), OMIM:617547)

Official abbreviation RDMS
Name dystrophy, retinal, with macular staphyloma
OMIM ID 617547
Human Phenotype Ontology Project (HPO) HPO
Inheritance Autosomal recessive
Individuals reported having this disease -
Phenotype entries for this disease -
Associated with 1 gene C21orf2
Associated tissues -
Disease features -
Remarks -
Date created 2020-11-11 10:13:25 +01:00 (CET)
Date last edited 2024-09-25 10:44:11 +02:00 (CEST)

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