eRAM
encyclopedia of Rare Disease Annotation for Precision Medicine
| lateral medullary syndrome | ||||
| Disease ID | 1216 |
|---|---|
| Disease | lateral medullary syndrome |
| Definition | INFARCTION of the dorsolateral aspect of MEDULLA OBLONGATA in the BRAIN STEM. It is caused by occlusion of the VERTEBRAL ARTERY and/or the posterior inferior cerebellar artery. Clinical manifestations vary with the size of infarction, but may include loss of pain and temperature sensation in the ipsilateral face and contralateral body below the chin; ipsilateral HORNER SYNDROME; ipsilateral ATAXIA; DYSARTHRIA; VERTIGO; nausea, hiccup; dysphagia; and VOCAL CORD PARALYSIS. (From Adams et al., Principles of Neurology, 6th ed, p801) |
| Synonym | dorsolateral medullary syndrome inferior cerebellar artery syndrome lateral bulbar syndrome lateral medullary syndrome [disease/finding] lateral medullary syndromes lms - lateral medullary syndrome medullary syndrome, dorsolateral posterior inferior cerebellar artery syndrome posterior inferior cerebellar artery syndrome (disorder) syndrome wallenberg syndrome, vieseaux-wallenberg syndrome, wallenberg syndromes, lateral medullary vieseaux wallenberg syndrome vieseaux-wallenberg syndrome vieusseux-wallenberg syndrome wallenberg syndrome wallenberg syndrome (disorder) wallenberg's syndrome wallenbergs syndrome |
| DOID | |
| UMLS | C0043019 |
| MeSH | |
| SNOMED-CT | |
| Comorbidity | UMLS | Disease | Sentences' Count(Total Sentences:6) C0019937 | horner syndrome | 1 C1959589 | cavernous angioma | 1 C0007786 | brain ischemia | 1 C0005697 | neurogenic bladder | 1 C0028738 | nystagmus | 1 C0022116 | ischemia | 1 |
| Curated Gene | Entrez_id | Symbol | Resource(Total Genes:1) |
| Inferring Gene | (Waiting for update.) |
| Text Mined Gene | Entrez_id | Symbol | Score | Resource(Total Genes:5) |
| Locus | (Waiting for update.) |
| Disease ID | 1216 |
|---|---|
| Disease | lateral medullary syndrome |
| Integrated Phenotype | (Waiting for update.) |
| Text Mined Phenotype | HPO | Name | Sentences' Count(Total Phenotypes:13) HP:0001269 | Hemiparesis | 2 HP:0002015 | Swallowing difficulty | 2 HP:0000011 | Neurogenic bladder | 1 HP:0002527 | Falls | 1 HP:0002277 | Horner's syndrome | 1 HP:0001048 | Cavernous angioma | 1 HP:0030322 | Vertebral artery hypoplasia | 1 HP:0000639 | Nystagmus | 1 HP:0002637 | Brain ischemia | 1 HP:0012044 | Seesaw nystagmus | 1 HP:0002321 | Vertigo | 1 HP:0002273 | Tetraparesis | 1 HP:0003401 | Paresthesia | 1 |
| Disease ID | 1216 |
|---|---|
| Disease | lateral medullary syndrome |
| Manually Symptom | UMLS | Name(Total Manually Symptoms:5) |
| Text Mined Symptom | UMLS | Name | Sentences' Count(Total Symptoms:3) |
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) | |
|---|---|
| (Waiting for update.) | |
GWASdb Snp Trait(Total Genotypes:0) | |
|---|---|
| (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 | 1216 |
|---|---|
| Disease | lateral medullary syndrome |
| Case | (Waiting for update.) |