Disease #05042 (SIFD (Sideroblastic anemia with B-cell immunodeficiency, periodic fevers, and developmental delay), OMIM:616084)
Official abbreviation |
SIFD |
Name |
Sideroblastic anemia with B-cell immunodeficiency, periodic fevers, and developmental delay |
OMIM ID |
616084 |
Human Phenotype Ontology Project (HPO) |
HPO |
Inheritance |
Autosomal recessive |
Individuals reported having this disease |
- |
Phenotype entries for this disease |
- |
Associated with 1 gene |
TRNT1 |
Associated tissues |
- |
Disease features |
- |
Remarks |
- |
Date created |
2015-09-23 11:00:40 +02:00 (CEST) |
Date last edited |
2021-12-10 21:51:32 +01:00 (CET) |
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