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Hereditary spherocytosis type 4

MONDO:0012981

Any hereditary spherocytosis in which the cause of the disease is a mutation in the SLC4A1 gene.

Also known as: HS4, SLC4A1 hereditary spherocytosis, SPH4, hereditary spherocytosis caused by mutation in SLC4A1, spherocytosis, hereditary, 4, spherocytosis, type 4

40 clinical trials for this condition and its sub-types.

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Broader categories

Disease (618) Anemia (203) Hereditary disease (172) Hematologic disorder (160) Hemolytic anemia (17) Human disease (14) Familial hemolytic anemia (3) Disease of genetic or genomic mechanism (2) Hereditary spherocytosis (2) Disease by body system or component (0)
Trials to join now! 19 Not yet recruiting 2 Not yet finished but already full! 5 Completed 13 Terminated 1
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  • Can extra care after transplant help older patients live better?

    Disease control Terminated

    This study tested two extra care programs—supportive palliative care and clinical management of other health issues—for older or frail patients who had a donor stem cell transplant. The goal was to see if these programs could improve quality of life and survival compared to stand…

    Phase: PHASE2, PHASE3 • Sponsor: Fred Hutchinson Cancer Center • Aim: Disease control

    Last updated Jun 27, 2026 08:10 UTC

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