OBO ID: DOID:0050649 |
Term Name: | atransferrinemia | Search Ontology: | |
---|---|---|---|
Synonyms: |
|
||
Definition: | A metal metabolism disorder that is characterized by transferrin deficiency, microcytic anemia, and iron loading, and has_material_basis_in autosomal recessive inheritance of homozygous or compound heterozygous mutation in the structural gene for transferrin (TF) on chromosome 3q22. (3) | ||
References: |
|
||
Ontology: | Human Disease ( DOID:0050649 ) |
OTHER atransferrinemia PAGES
ZEBRAFISH MODELS
No data available
PHENOTYPE
No data available
CITATIONS: None
Your Input Welcome
Thank you for submitting comments. Your input has been emailed to ZFIN curators who may contact you if
additional information is required.
Oops. Something went wrong. Please try again later.