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)

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