Portal:RareDisease/News
From WikiPathways
(Difference between revisions)
| Line 7: | Line 7: | ||
* [[:Pathway:WP4299|Lamin A-processing pathway]] | * [[:Pathway:WP4299|Lamin A-processing pathway]] | ||
* [[:Pathway:WP4298|Viral Acute Myocarditis]] | * [[:Pathway:WP4298|Viral Acute Myocarditis]] | ||
| + | * [[:Pathway:WP4156|Disorders of Phenylalanine and Tetrahydrobiopterin (BH4) Metabolism]] | ||
| + | * [[:Pathway:WP4506|Tyrosine Metabolism]] | ||
| + | * [[:Pathway:WP4292|Sulphur Amino Acids]] | ||
| + | * [[:Pathway:WP4259|Disorders of Folate Metabolism and Transport]] | ||
| + | * [[:Pathway:WP4288|MTHFR deficiency (additional pathway)]] | ||
| + | * [[:Pathway:WP4228|Vitamine B6-Dependent and Responsive Disorders]] | ||
| + | * [[:Pathway:WP4507|Molybdenum (Moco) cofactor biosynthesis]] | ||
| + | * [[:Pathway:WP4504|Cysteine and Methionine catabolism]] | ||
| + | * [[:Pathway:WP4271|Vitamin B12 Disorders]] | ||
| + | * [[:Pathway:WP4297|Thiamine Disorders]] | ||
Revision as of 14:24, 30 January 2019
Explore rare disease pathways on WikiPathways:
- MECP2 and Associated Rett Syndrome
- Amyotrophic lateral sclerosis (ALS) SOD1 - CHMP2B MODEL
- 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 (BH4) Metabolism
- Tyrosine Metabolism
- Sulphur Amino Acids
- Disorders of Folate Metabolism and Transport
- MTHFR deficiency (additional pathway)
- Vitamine B6-Dependent and Responsive Disorders
- Molybdenum (Moco) cofactor biosynthesis
- Cysteine and Methionine catabolism
- Vitamin B12 Disorders
- Thiamine Disorders
