Diseases by genes

DISEASE GENE
Acatalasemia
Acyl-CoA oxidase deficiency (Pseudoneonatal adrenoleukodystrophy)
Adult-onset sensory motor neuropathy
Amyotrophic lateral sclerosis, ALS1
Bifunctional protein deficiency
Contiguous ABCD1/DXS1375E deletion syndrome
Glomerulosclerosis
Glutaric aciduria type III No gene found
Hyperoxaluria type I
Infantile Refsum disease
Malonic aciduria
Mental retardation X-linked 63, MRX63
Mulibrey nanism
Neonatal adrenoleukodystrophy
Refsum disease
Rhizomelic chondrodysplasia punctata type 1 (RCDP1 )
Rhizomelic chondrodysplasia punctata type 2 (RCDP2)
Rhizomelic chondrodysplasia punctata type 3 (RCDP3)
Sjogren-Larsson syndrome
X-linked adrenoleukodystrophy
Xanthinuria
Zellweger syndrome