Portal:RareDisease/FeaturedPathways

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MECP2 and Associated Rett Syndrome (Homo sapiens)
Amyotrophic lateral sclerosis (ALS) (Homo sapiens)
Fanconi Anemia Pathway (Homo sapiens)
The effect of progerin on the involved genes in Hutchinson-Gilford Progeria Syndrome (Homo sapiens)
Lamin A-processing pathway (Homo sapiens)
Viral Acute Myocarditis (Homo sapiens)
Disorders of Phenylalanine and Tetrahydrobiopterin (BH4) Metabolism
Tyrosine Metabolism
Sulphur Amino Acids
Disorders of Folate Metabolism and Transport
MTHFR deficiency (additonal pathway)
Vitamine B6-Dependent and Responsive Disorders
Molybdenum (Moco) cofactor biosynthesis
Cysteine and Methionine catabolism
Vitamin B12 Disorders
Thiamine Disorders
Disorders of the Krebs Cycle
Lysosomal Storage Disorders Including Neuronal Ceroid Lipofuscinoses
Neurotransmitter Disorders
Purine Disorders
Pyrimidine Disorders

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