Portal:RareDisease/News
From WikiPathways
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* [[Pathway:WP4657|22q11.2 Deletion Syndrome]] | * [[Pathway:WP4657|22q11.2 Deletion Syndrome]] | ||
* [[Pathway:WP4746|Thyroid hormones production and their peripheral downstream signalling effects regarding congenital hypothyroidism]] | * [[Pathway:WP4746|Thyroid hormones production and their peripheral downstream signalling effects regarding congenital hypothyroidism]] | ||
| + | * [[Pathway:WP4656|Joubert Syndrome]] | ||
Revision as of 12:49, 28 November 2019
Explore rare disease pathways on WikiPathways:
- MECP2 and Associated Rett Syndrome
- Amyotrophic lateral sclerosis (ALS)
- Fanconi Anemia Pathway
- The effect of progerin on the involved genes in Hutchinson-Gilford Progeria Syndrome
- Lamin A-processing pathway
- Viral Acute Myocarditis
- Disorders of Phenylalanine and Tetrahydrobiopterin
- Tyrosine Metabolism
- Sulphur Amino Acids
- Disorders of Folate Metabolism and Transport
- MTHFR deficiency
- Vitamine B6-Dependent and Responsive Disorders
- Molybdenum (Moco) cofactor biosynthesis
- Cysteine and Methionine catabolism disorders
- Vitamin B12 Disorders
- Thiamine Disorders
- Disorders of the Krebs Cycle
- Lysosomal Storage Disorders Including Neuronal Ceroid Lipofuscinoses
- Neurotransmitter Disorders
- Purine Disorders
- Pyrimidine Disorder
- Pathways Regulating Hippo Signaling
- po-Merlin Signaling Dysregulation
- Gamma-Glutamyl Cycle for the biosynthesis and degradation of glutathione, including diseases
- Cerebral Organic Acidurias
- Glycosylation and related congenital defects
- Metabolic pathway of LDL, HDL and TG
- Classical pathway of steroidogenesis, including diseases
- The alternative pathway of fetal androgen synthesis
- Fragile X Syndrome
- WDR45 autophagy related pathway
- Rett syndrome causing genes
- Prion disease pathway
- ERK Pathway in Huntington's Disease
- Envelope proteins and their potential roles in EDMD physiopathology
- Parkinsons Disease Pathway
- Alzheimers Disease
- 22q11.2 Deletion Syndrome
- Thyroid hormones production and their peripheral downstream signalling effects regarding congenital hypothyroidism
- Joubert Syndrome
