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GTR Home > Conditions/Phenotypes > Atransferrinemia

Atransferrinemia

Synonyms: Familial hypotransferrinemia

Summary

Absence of transferrin, a protein that transports iron, in the blood. [from HPO]

Available tests

25 tests are in the database for this condition.

Check Related conditions for additional relevant tests.

Clinical tests (24 available)

Molecular Genetics Tests

Research tests

See all research tests for this condition (1)

Genes See tests for all associated and related genes

Associated genes Help
Genes reported to contribute to the condition.

TF
36 tests
Also known as: HEL-S-71p, PRO1557, PRO2086, TFQTL1, TF
Summary: transferrin

Imported from Human Phenotype Ontology (HPO)

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Abnormality of blood and blood-forming tissues
- Hypochromic anemia
  Hypochromic anemia
  - MedGen UID: 8065
  - Concept ID: C0002884
  - Finding: Disease or Syndrome
  Abnormality of blood and blood-forming tissues
  See: Feature record | Search on this feature
Abnormality of metabolism/homeostasis
- Atransferrinemia
  Atransferrinemia
  - MedGen UID: 105489
  - Concept ID: C0521802
  - Finding: Disease or Syndrome
  Abnormality of metabolism/homeostasis
  See: Feature record | Search on this feature
Abnormality of the cardiovascular system
- Congestive heart failure
  Congestive heart failure
  - MedGen UID: 9169
  - Concept ID: C0018802
  - Finding: Disease or Syndrome
  Abnormality of the cardiovascular system
  See: Feature record | Search on this feature
Abnormality of the digestive system
- Abnormality of the liver
  Abnormality of the liver
  - MedGen UID: 893061
  - Concept ID: C4021780
  - Finding: Finding
  Abnormality of the digestive system
  See: Feature record | Search on this feature

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Clinical resources

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