| SelfDecode | Genome Analysis

Disease
Amyotrophic Lateral Sclerosis 2, Juvenile
Charcot-Marie-Tooth Disease, Type 4b2
Crohn's Disease
Hereditary Spastic Paralysis, Infantile Onset Ascending
Primary Biliary Cirrhosis
Macrocephaly, Alopecia, Cutis Laxa, And Scoliosis
Martsolf Syndrome
Osteitis Deformans
Primary Lateral Sclerosis Juvenile
Warburg Sjo Fledelius Syndrome

Rab Guanyl-Nucleotide Exchange Factor Activity