eRAM
encyclopedia of Rare Disease Annotation for Precision Medicine
| reflex sympathetic dystrophy | ||||
| Disease ID | 1363 |
|---|---|
| Disease | reflex sympathetic dystrophy |
| Definition | A syndrome characterized by severe burning pain in an extremity accompanied by sudomotor, vasomotor, and trophic changes in bone without an associated specific nerve injury. This condition is most often precipitated by trauma to soft tissue or nerve complexes. The skin over the affected region is usually erythematous and demonstrates hypersensitivity to tactile stimuli and erythema. (Adams et al., Principles of Neurology, 6th ed, p1360; Pain 1995 Oct;63(1):127-33) |
| Synonym | algodystrophy algodystrophy (disorder) algoneurodystrophy atrophies, sudek's atrophy, sudek atrophy, sudek's complex regional pain syndrome i complex regional pain syndrome type i complex regional pain syndrome type i of the upper limb complex regional pain syndrome, type i cprs type i cprs type is crps - complex regional pain syndrome type i crps i crps type i dystrophies, reflex sympathetic dystrophy, reflex sympathetic hand shoulder syndrome is, cprs type pain syndrome type i, complex regional pain syndrome type i, regional, complex reflex dystrophia, sympathetic reflex neurovascular dystrophy reflex sympathetic dystrophies reflex sympathetic dystrophy (& sudek's atrophy) reflex sympathetic dystrophy (& sudek's atrophy) (disorder) reflex sympathetic dystrophy (disorder) reflex sympathetic dystrophy [ambiguous] reflex sympathetic dystrophy [disease/finding] reflex sympathetic dystrophy of the upper limb reflex sympathetic dystrophy of upper extremity reflex sympathetic dystrophy of upper extremity (disorder) reflex sympathetic dystrophy syndrome reflex sympathetic dystrophy syndrome (rsds) reflex sympathetic dystrophy, unspecified rflx sym dystrph up limb rnd rsd (reflex sympathetic dystrophy) rsd - reflex sympathetic dystrophy rsds rsds (reflex sympathetic dystrophy) shoulder hand syndrome shoulder-hand syndrome shoulder-hand syndrome (disorder) shoulder-hand syndromes steinbrocker syndrome steinbrocker's syndrome sudeck's atrophy sudeck's atrophy (disorder) sudeck's syndrome sudek atrophy sudek's atrophies sudek's atrophy sudek's atrophy (disorder) sudeks atrophy sympathetic dystrophies, reflex sympathetic dystrophy, reflex sympathetic reflex dystrophia sympathetic reflex dystrophias syndrome, reflex sympathetic dystrophy syndrome, shoulder-hand syndromes, shoulder-hand type i complex regional pain syndrome type i, cprs type is, cprs unsp rflx sympth dystrph |
| Orphanet | |
| OMIM | |
| DOID | |
| UMLS | C0034931 |
| MeSH | |
| SNOMED-CT | |
| Comorbidity | UMLS | Disease | Sentences' Count(Total Sentences:13) C0013421 | dystonia | 2 C0017653 | glomus tumor | 2 C0149931 | migraine | 1 C0024408 | joseph disease | 1 C0032371 | poliomyelitis | 1 C0041696 | major depressive disorder | 1 C0011570 | depression | 1 C0278678 | metastatic renal cell carcinoma | 1 C0018991 | hemiplegia | 1 C0007134 | renal cell carcinoma | 1 C0026850 | muscular dystrophy | 1 C0024408 | machado-joseph disease | 1 C0038013 | ankylosing spondylitis | 1 |
| Curated Gene | (Waiting for update.) |
| Inferring Gene | (Waiting for update.) |
| Text Mined Gene | Entrez_id | Symbol | Score | Resource(Total Genes:27) 632 | BGLAP | 1.359 | DISEASES 796 | CALCA | 5.358 | DISEASES 796 | CALCA | 2.424 | DISEASES 959 | CD40LG | 1.068 | DISEASES 1312 | COMT | 1.012 | DISEASES 1813 | DRD2 | 1.203 | DISEASES 10938 | EHD1 | 2.106 | DISEASES 2316 | FLNA | 1.169 | DISEASES 2556 | GABRA3 | 3.228 | DISEASES 728441 | GGT2 | 3.022 | DISEASES 2719 | GPC3 | 1.336 | DISEASES 2821 | GPI | 2.213 | DISEASES 8518 | IKBKAP | 1.415 | DISEASES 102723508 | KANTR | 1.834 | DISEASES 286826 | LIN9 | 5.217 | DISEASES 4803 | NGF | 1.771 | DISEASES 594857 | NPS | 3.692 | DISEASES 4988 | OPRM1 | 1.664 | DISEASES 55010 | PARPBP | 3.175 | DISEASES 5333 | PLCD1 | 3.197 | DISEASES 51334 | PRR16 | 2.82 | DISEASES 29122 | PRSS50 | 3.06 | DISEASES 5817 | PVR | 1.119 | DISEASES 6164 | RPL34 | 1.941 | DISEASES 6863 | TAC1 | 2.748 | DISEASES 7432 | VIP | 1.017 | DISEASES 7694 | ZNF135 | 2.751 | DISEASES |
| Locus | (Waiting for update.) |
| Disease ID | 1363 |
|---|---|
| Disease | reflex sympathetic dystrophy |
| Integrated Phenotype | (Waiting for update.) |
| Text Mined Phenotype | HPO | Name | Sentences' Count(Total Phenotypes:12) HP:0012531 | Pain | 7 HP:0001332 | Dystonia | 2 HP:0005584 | Renal cell carcinoma | 1 HP:0002301 | Hemiplegia | 1 HP:0100022 | Movement disorder | 1 HP:0002960 | Autoimmune condition | 1 HP:0003560 | Muscular dystrophy | 1 HP:0002076 | Migraine headaches | 1 HP:0000969 | Dropsy | 1 HP:0001297 | Cerebral vascular events | 1 HP:0000716 | Depression | 1 HP:0002664 | Neoplasia | 1 |
| Disease ID | 1363 |
|---|---|
| Disease | reflex sympathetic dystrophy |
| Manually Symptom | UMLS | Name(Total Manually Symptoms:17) C2676454 | h syndrome C2598155 | pain C2364114 | tremor C2220255 | motor disturbances C1660219 | analgesia C1253936 | synovial effusion C0426768 | o sign C0393593 | dystonia C0311223 | frozen shoulder C0240182 | leuconychia C0206732 | epithelioid hemangioendothelioma C0030200 | intractable pain C0027073 | myofascial pain syndrome C0026650 | movement disorder C0022408 | arthropathy C0018924 | hemarthrosis C0013384 | abnormal movements |
| Text Mined Symptom | UMLS | Name | Sentences' Count(Total Symptoms:2) |
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 | 1363 |
|---|---|
| Disease | reflex sympathetic dystrophy |
| Case | (Waiting for update.) |