Disease #01655 (SIDBA2 (anemia, sideroblastic, type 2, pyridoxine-refractory (SIDBA-2)), OMIM:205950)
Official abbreviation |
SIDBA2 |
Name |
anemia, sideroblastic, type 2, pyridoxine-refractory (SIDBA-2) |
OMIM ID |
205950 |
Human Phenotype Ontology Project (HPO) |
HPO |
Inheritance |
Autosomal recessive |
Individuals reported having this disease |
- |
Phenotype entries for this disease |
- |
Associated with 1 gene |
SLC25A38 |
Associated tissues |
- |
Disease features |
autosomal recessive |
Remarks |
- |
Date created |
2014-09-25 23:29:40 +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.
|