P3H3
Description
The P3H3 (prolyl 3-hydroxylase 3) is a protein-coding gene located on chromosome 12.
P3H3 is also known as GRCB, HSU47926, LEPREL2.
Associated Diseases
- microcytic anemia with liver iron overload
- hemoglobin E-beta-thalassemia syndrome
- dehydrated hereditary stomatocytosis
- hemoglobin D disease
- familial pseudohyperkalemia
- hemochromatosis type 5
- hemolytic anemia due to erythrocyte adenosine deaminase overproduction
- IRIDA syndrome
- cryohydrocytosis
- hemoglobin E disease
- hypoparathyroidism, familial isolated, 2
- monosomy 7 myelodysplasia and leukemia syndrome 1
- delta-beta-thalassemia
- hereditary elliptocytosis
- Rh deficiency syndrome
- overhydrated hereditary stomatocytosis
- elliptocytosis 2
