PALMD
Description
The PALMD (palmdelphin) is a protein-coding gene located on chromosome 1.
PALMD is also known as C1orf11, PALML.
Associated Diseases
- congenital anomaly of the great arteries
- congenital bilateral aplasia of vas deferens from CFTR mutation
- Griscelli syndrome type 3
- vasculitis, lymphocytic, nodular
- uncombable hair syndrome
- oculocutaneous albinism type 3
- hypotrichosis simplex
- ermine phenotype
- Tietz syndrome
