OBO ID: DOID:0050649
Term Name: atransferrinemia Search Ontology:
Synonyms:
  • familial hypotransferrinemia
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
GENES INVOLVED
Human Gene Zebrafish Ortholog OMIM Term OMIM Phenotype ID
TF Atransferrinemia 209300
ZEBRAFISH MODELS No data available
PHENOTYPE No data available

CITATIONS: None