LELP1
Description
The LELP1 (late cornified envelope like proline rich 1) is a protein-coding gene located on chromosome 1.
LELP1 is also known as -.
Associated Diseases
- hereditary persistence of fetal hemoglobin-sickle cell disease syndrome
- alpha-thalassemia-myelodysplastic syndrome
- hemoglobin D disease
- alpha thalassemia-intellectual disability syndrome type 1
- X-linked sideroblastic anemia 1
- hemoglobin E-beta-thalassemia syndrome
- X-linked severe congenital neutropenia
- myeloperoxidase deficiency
- delta-beta-thalassemia
- hemoglobin E disease
- dominant beta-thalassemia
- hemoglobin C-beta-thalassemia syndrome
- monosomy 7 myelodysplasia and leukemia syndrome 1
- neutropenia, severe congenital, 2, autosomal dominant
- monosomy 7 myelodysplasia and leukemia syndrome 2
