Disease #05731 (MYP26 (myopia, type 26, X-linked, female-limited (MYP26)), OMIM:301010)

Official abbreviation MYP26
Name myopia, type 26, X-linked, female-limited (MYP26)
OMIM ID 301010
Human Phenotype Ontology Project (HPO) HPO
Inheritance X-linked
Individuals reported having this disease -
Phenotype entries for this disease -
Associated with 1 gene ARR3
Associated tissues -
Disease features -
Remarks -
Date created 2020-04-24 12:27:56 +02:00 (CEST)
Date last edited 2021-12-10 21:51:32 +01:00 (CET)

Screenscraping/webscraping (downloading large amounts of data using scripts) is strictly prohibited.
Use our APIs to retrieve data.