Contact us   |  

Members

Information

Atoyebi, Wale

About me

Name: Wale

Surname: Atoyebi

Academic title: Consultant Haematologist and Honorary Clinical Lecturer


Which is your area of expertise for the "Disease/group of diseases"?

  • Diagnostics
  • Treatment and care

Specify your expertise for the "Disease/group of diseases" (eg SCT, Molecular diagnosis):

Molecular diagnosis, treatment

Diseases:

Rare hereditary hemochromatosis HFE related hereditary hemochromatosis Symptomatic form of hemochromatosis type 1 (OMIM 235200) Hemochromatosis due to rare mutations in HFE (OMIM 235200) Non-HFE related hereditary hemochromatosis Hemochromatosis type 2(OMIM 602390, 613313) Hemochromatosis type 2A (OMIM 602390) Hemochromatosis type 2B (OMIM 613313) Hemochromatosis type 3 (OMIM 604250) Hemochromatosis type 5 (OMIM 615517) Hemochromatosis type 4B (OMIM 606069) Ferroportin Disease Hemochromatosis type 4A (OMIM 606069)


Subnetwork representative:

  • HH-Iron

Member Go to member

Name english: Oxford University Hospitals NHS Foundation Trust

Name original: Oxford University Hospitals NHS Foundation Trust


Healthcare provider Go to healthcare provider

Name english: Oxford University Hospitals NHS Foundation Trust

Name original: Oxford University Hospitals NHS Foundation Trust

Departments

English name Original name Subnetworks of expertise Healthcare provider