Portal:RareDisease/News
From WikiPathways
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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:WP4153|Lysosomal Storage Disorders Including Neuronal Ceroid Lipofuscinoses]] | * [[Pathway:WP4153|Lysosomal Storage Disorders Including Neuronal Ceroid Lipofuscinoses]] | ||
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* [[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: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:WP4656|Joubert Syndrome]] | * [[Pathway:WP4656|Joubert Syndrome]] | ||
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* [[Pathway:WP4844|The influence of laminopathies on Wnt signaling]] | * [[Pathway:WP4844|The influence of laminopathies on Wnt signaling]] | ||
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* [[Pathway:WP4838|Regucalcin in proximal tubule epithelial kidney cells]] | * [[Pathway:WP4838|Regucalcin in proximal tubule epithelial kidney cells]] | ||
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* [[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:WP4823|Genes controlling renal nephrogenesis]] | * [[Pathway:WP4823|Genes controlling renal nephrogenesis]] | ||
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* [[Pathway:WP4879|Interacting Laminopathic Pathways]] | * [[Pathway:WP4879|Interacting Laminopathic Pathways]] | ||
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| + | Inborn errors of metabolism | ||
| + | * [[Pathway:WP4220|Neurotransmitter Disorders]] | ||
| + | * [[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]] | ||
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| + | 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]] | ||
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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:
- 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
- Lysosomal Storage Disorders Including Neuronal Ceroid Lipofuscinoses
- Pathways Regulating Hippo Signaling
- po-Merlin Signaling Dysregulation
- 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
- Joubert Syndrome
- The influence of laminopathies on Wnt signaling
- Regucalcin in proximal tubule epithelial kidney cells
- GDNF/RET signalling axis
- Conversion of Angiotensinogen to Angiotensin II
- Genes controlling renal nephrogenesis
- Interacting Laminopathic Pathways
Inborn errors of metabolism
- Neurotransmitter Disorders
- Purine Disorders
- Pyrimidine Disorder
- Purine metabolism
- Thyroid hormones production and their peripheral downstream signalling effects regarding congenital hypothyroidism
- 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
- 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
Disorders of sex development and fertility
- Genes involved in male infertility
- The alternative pathway of fetal androgen synthesis
- Somatic Sex determination
- Mammalian disorder of sexual development
- Kisspeptin/Kisspeptin Receptor System in the Ovary
- Peroxiredoxin 2 induced ovarian failure
Copy number variation syndromes (CNVs) - duplications or deletions
