Spherocytosis, Type 4; Sph4
Table of contents:
Clinical Features
Phenotypes and symptoms related to Spherocytosis, Type 4; Sph4
- Anemia
- Splenomegaly
- Jaundice
- Hemolytic anemia
- Hyperbilirubinemia
- Reticulocytosis
- Spherocytosis
- Increased red cell osmotic fragility
Incidence and onset information
— Currently we don't have prevalence information about this disease (Not enough data available about incidence and published cases.)— No data available about the known clinical features onset.
Alternative names
Spherocytosis, Type 4; Sph4 Is also known as hs4, spherocytosis, hereditary, 4.
Researches and researchers
Currently, we don't have any information about doctors, researches or researchers related to this disease. Please contact us if you would like to appear here.Sources and references
You can check the following sources for additional information.
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