Disease #05253 (ATFB18 (fibrillation, atrial, familial, type 18 (ATFB-18)), OMIM:617280)

Official abbreviation ATFB18
Name fibrillation, atrial, familial, type 18 (ATFB-18)
OMIM ID 617280
Human Phenotype Ontology Project (HPO) HPO
Inheritance Autosomal dominant
Individuals reported having this disease -
Phenotype entries for this disease -
Associated with 1 gene MYL4
Associated tissues -
Disease features -
Remarks -
Date created 2017-03-31 14:15:27 +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.