eRAM
encyclopedia of Rare Disease Annotation for Precision Medicine
| causalgia | ||||
| Disease ID | 1700 |
|---|---|
| Disease | causalgia |
| Definition | A complex regional pain syndrome characterized by burning pain and marked sensitivity to touch (HYPERESTHESIA) in the distribution of an injured peripheral nerve. Autonomic dysfunction in the form of sudomotor (i.e., sympathetic innervation to sweat glands), vasomotor, and trophic skin changes may also occur. (Adams et al., Principles of Neurology, 6th ed, p1359) |
| Synonym | causalgia (disorder) causalgia (finding) causalgia [disease/finding] causalgia nos causalgia syndrome causalgia syndromes complex regional pain syndrome ii complex regional pain syndrome type ii complex regional pain syndrome, type ii complex regional pain syndrome, type ii (disorder) crps - complex regional pain syndrome type ii crps ii crps type ii deafferentation pain erythromelalgia, traumatic pain, deafferentation syndrome, causalgia syndromes, causalgia type ii complex regional pain syndrome weir mitchell causalgia |
| Orphanet | |
| DOID | |
| UMLS | C0007462 |
| MeSH | |
| SNOMED-CT | |
| Comorbidity | UMLS | Disease | Sentences' Count(Total Sentences:2) |
| Curated Gene | (Waiting for update.) |
| Inferring Gene | (Waiting for update.) |
| Text Mined Gene | Entrez_id | Symbol | Score | Resource(Total Genes:12) 796 | CALCA | 3.368 | DISEASES 2668 | GDNF | 1.772 | DISEASES 3440 | IFNA2 | 1.524 | DISEASES 8972 | MGAM | 1.286 | DISEASES 4803 | NGF | 2.686 | DISEASES 594857 | NPS | 2.487 | DISEASES 4914 | NTRK1 | 1.847 | DISEASES 6336 | SCN10A | 2.152 | DISEASES 9467 | SH3BP5 | 2.869 | DISEASES 6863 | TAC1 | 2.734 | DISEASES 7316 | UBC | 2.671 | DISEASES 7694 | ZNF135 | 3.431 | DISEASES |
| Locus | (Waiting for update.) |
| Disease ID | 1700 |
|---|---|
| Disease | causalgia |
| Integrated Phenotype | (Waiting for update.) |
| Text Mined Phenotype | HPO | Name | Sentences' Count(Total Phenotypes:2) |
| Disease ID | 1700 |
|---|---|
| Disease | causalgia |
| Manually Symptom | UMLS | Name(Total Manually Symptoms:2) |
| Text Mined Symptom | UMLS | Name | Sentences' Count(Total Symptoms:1) |
Manually Genotype(Total Text Mining Genotypes:0) |
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| (Waiting for update.) |
Text Mining Genotype(Total Genotypes:0) | |
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| (Waiting for update.) | |
All Snps(Total Genotypes:0) | |
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| (Waiting for update.) | |
GWASdb Annotation(Total Genotypes:0) | |
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| (Waiting for update.) | |
GWASdb Snp Trait(Total Genotypes:0) | |
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| (Waiting for update.) | |
Mapped by lexical matching(Total Items:0) |
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| (Waiting for update.) |
Mapped by homologous gene(Total Items:0) |
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| (Waiting for update.) |
| Disease ID | 1700 |
|---|---|
| Disease | causalgia |
| Case | (Waiting for update.) |