Disease #05444 (SIDBA3 (anemia, sideroblastic, type 3 (SIDBA-3)), OMIM:616860)

Official abbreviation SIDBA3
Name anemia, sideroblastic, type 3 (SIDBA-3)
OMIM ID 616860
Human Phenotype Ontology Project (HPO) HPO
Inheritance Autosomal recessive
Individuals reported having this disease -
Phenotype entries for this disease -
Associated with 1 gene GLRX5
Associated tissues -
Disease features autosomal recessive
Remarks -
Date created 2018-06-22 10:38:32 +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.