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) HJV related hereditary hemochromatosis - OMIM 602390 (Hemochromatosis type 2A) HAMP related hereditary hemochromatosis - OMIM 613313 (Hemochromatosis type 2B) TFR2 related hereditary hemochromatosis OMIM 604250 (Hemochromatosis type 3) FTH related hereditary hemochromatosis - OMIM 615517 (Hemochromatosis type 5) Ferroportin Disease (Hemochromatosis type 4B)​ SLC40A1 related hereditary hemochromatosis - OMIM 606069 (Hemochromatosis type 4A)


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