C19orf81
Description
The C19ORF81 (chromosome 19 open reading frame 81) is a protein-coding gene located on chromosome 19.
C19ORF81 is also known as -.
Associated Diseases
- hypotrichosis simplex
- primary familial polycythemia due to EPO receptor mutation
- uncombable hair syndrome
- wooly hair, autosomal recessive 3
- hypotrichosis 4
- hemolytic anemia due to diphosphoglycerate mutase deficiency
- alopecia universalis congenita
- trichodysplasia-xeroderma syndrome
- erythrocytosis, familial, 3
- erythrocytosis, familial, 6
- X-linked sideroblastic anemia 1
- Marie Unna hereditary hypotrichosis
- hypotrichosis
- delta-beta-thalassemia
- alopecia, androgenetic, 1
- monilethrix
- T-cell immunodeficiency, congenital alopecia, and nail dystrophy
- autosomal dominant wooly hair
- isolated anterior cervical hypertrichosis
- Ambras type hypertrichosis universalis congenita
