Portal:RareDisease/News

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* [[Pathway:WP4299|Lamin A-processing pathway]]
* [[Pathway:WP4299|Lamin A-processing pathway]]
* [[Pathway:WP4298|Viral Acute Myocarditis]]
* [[Pathway:WP4298|Viral Acute Myocarditis]]
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* [[Pathway:WP4156|Disorders of Phenylalanine and Tetrahydrobiopterin]]
 
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* [[Pathway:WP4506|Tyrosine Metabolism]]
 
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* [[Pathway:WP4292|Sulphur Amino Acids]]
 
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* [[Pathway:WP4259|Disorders of Folate Metabolism and Transport]]
 
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* [[Pathway:WP4288|MTHFR deficiency]]
 
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* [[Pathway:WP4228|Vitamine B6-Dependent and Responsive Disorders]]
 
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* [[Pathway:WP4507|Molybdenum (Moco) cofactor biosynthesis]]
 
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* [[Pathway:WP4504|Cysteine and Methionine catabolism disorders]]
 
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* [[Pathway:WP4271|Vitamin B12 Disorders]]
 
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* [[Pathway:WP4297|Thiamine Disorders]]
 
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* [[Pathway:WP4236|Disorders of the Krebs Cycle]]
 
* [[Pathway:WP4153|Lysosomal Storage Disorders Including Neuronal Ceroid Lipofuscinoses]]
* [[Pathway:WP4153|Lysosomal Storage Disorders Including Neuronal Ceroid Lipofuscinoses]]
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* [[Pathway:WP4220|Neurotransmitter Disorders]]
 
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* [[Pathway:WP4224|Purine Disorders]]
 
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* [[Pathway:WP4225|Pyrimidine Disorder]]
 
* [[Pathway:WP4540|Pathways Regulating Hippo Signaling]]
* [[Pathway:WP4540|Pathways Regulating Hippo Signaling]]
* [[Pathway:WP4541|po-Merlin Signaling Dysregulation]]
* [[Pathway:WP4541|po-Merlin Signaling Dysregulation]]
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* [[Pathway:WP4518|Gamma-Glutamyl Cycle for the biosynthesis and degradation of glutathione, including diseases]]
 
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* [[Pathway:WP4519|Cerebral Organic Acidurias]]
 
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* [[Pathway:WP4521|Glycosylation and related congenital defects]]
 
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* [[Pathway:WP4522|Metabolic pathway of LDL, HDL and TG]]
 
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* [[Pathway:WP4523|Classical pathway of steroidogenesis, including diseases]]
 
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* [[Pathway:WP4524|The alternative pathway of fetal androgen synthesis]]
 
* [[Pathway:WP4549|Fragile X Syndrome]]
* [[Pathway:WP4549|Fragile X Syndrome]]
* [[Pathway:WP4577|WDR45 autophagy related pathway]]
* [[Pathway:WP4577|WDR45 autophagy related pathway]]
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* [[Pathway:WP2371|Parkinsons Disease Pathway]]
* [[Pathway:WP2371|Parkinsons Disease Pathway]]
* [[Pathway:WP2059|Alzheimers Disease]]
* [[Pathway:WP2059|Alzheimers Disease]]
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* [[Pathway:WP4746|Thyroid hormones production and their peripheral downstream signalling effects regarding congenital hypothyroidism]]
 
* [[Pathway:WP4656|Joubert Syndrome]]
* [[Pathway:WP4656|Joubert Syndrome]]
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* [[Pathway:WP4673|Genes involved in male infertility]]
 
* [[Pathway:WP4844|The influence of laminopathies on Wnt signaling]]
* [[Pathway:WP4844|The influence of laminopathies on Wnt signaling]]
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* [[Pathway:WP4842|Mammalian disorder of sexual development]]
 
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* [[Pathway:WP4871|Kisspeptin/Kisspeptin Receptor System in the Ovary]]
 
* [[Pathway:WP4838|Regucalcin in proximal tubule epithelial kidney cells]]
* [[Pathway:WP4838|Regucalcin in proximal tubule epithelial kidney cells]]
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* [[Pathway:WP4835|Peroxiredoxin 2 induced ovarian failure]]
 
* [[Pathway:WP4830|GDNF/RET signalling axis]]
* [[Pathway:WP4830|GDNF/RET signalling axis]]
* [[Pathway:WP4818|Conversion of Angiotensinogen to Angiotensin II]]
* [[Pathway:WP4818|Conversion of Angiotensinogen to Angiotensin II]]
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* [[Pathway:WP4792|Purine metabolism]]
 
* [[Pathway:WP4823|Genes controlling renal nephrogenesis]]
* [[Pathway:WP4823|Genes controlling renal nephrogenesis]]
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* [[Pathway:WP4814|Somatic Sex determination]]
 
* [[Pathway:WP4879|Interacting Laminopathic Pathways]]
* [[Pathway:WP4879|Interacting Laminopathic Pathways]]
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 +
Inborn errors of metabolism
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* [[Pathway:WP4220|Neurotransmitter Disorders]]
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* [[Pathway:WP4224|Purine Disorders]]
 +
* [[Pathway:WP4225|Pyrimidine Disorder]]
 +
* [[Pathway:WP4792|Purine metabolism]]
 +
* [[Pathway:WP4746|Thyroid hormones production and their peripheral downstream signalling effects regarding congenital hypothyroidism]]
 +
* [[Pathway:WP4518|Gamma-Glutamyl Cycle for the biosynthesis and degradation of glutathione, including diseases]]
 +
* [[Pathway:WP4519|Cerebral Organic Acidurias]]
 +
* [[Pathway:WP4521|Glycosylation and related congenital defects]]
 +
* [[Pathway:WP4522|Metabolic pathway of LDL, HDL and TG]]
 +
* [[Pathway:WP4523|Classical pathway of steroidogenesis, including diseases]]
 +
* [[Pathway:WP4156|Disorders of Phenylalanine and Tetrahydrobiopterin]]
 +
* [[Pathway:WP4506|Tyrosine Metabolism]]
 +
* [[Pathway:WP4292|Sulphur Amino Acids]]
 +
* [[Pathway:WP4259|Disorders of Folate Metabolism and Transport]]
 +
* [[Pathway:WP4288|MTHFR deficiency]]
 +
* [[Pathway:WP4228|Vitamine B6-Dependent and Responsive Disorders]]
 +
* [[Pathway:WP4507|Molybdenum (Moco) cofactor biosynthesis]]
 +
* [[Pathway:WP4504|Cysteine and Methionine catabolism disorders]]
 +
* [[Pathway:WP4271|Vitamin B12 Disorders]]
 +
* [[Pathway:WP4297|Thiamine Disorders]]
 +
* [[Pathway:WP4236|Disorders of the Krebs Cycle]]
 +
 +
Disorders of sex development and fertility
 +
* [[Pathway:WP4673|Genes involved in male infertility]]
 +
* [[Pathway:WP4524|The alternative pathway of fetal androgen synthesis]]
 +
* [[Pathway:WP4814|Somatic Sex determination]]
 +
* [[Pathway:WP4842|Mammalian disorder of sexual development]]
 +
* [[Pathway:WP4871|Kisspeptin/Kisspeptin Receptor System in the Ovary]]
 +
* [[Pathway:WP4835|Peroxiredoxin 2 induced ovarian failure]]
 +
Copy number variation syndromes (CNVs) - duplications or deletions
Copy number variation syndromes (CNVs) - duplications or deletions
* [[Pathway:WP4905|1q21.1 copy number variation syndrome]]
* [[Pathway:WP4905|1q21.1 copy number variation syndrome]]

Revision as of 15:10, 30 April 2020

Explore rare disease pathways on WikiPathways:

Inborn errors of metabolism

Disorders of sex development and fertility

Copy number variation syndromes (CNVs) - duplications or deletions

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