eRAM
encyclopedia of Rare Disease Annotation for Precision Medicine
| plummer vinson syndrome | ||||
| Disease ID | 1754 |
|---|---|
| Disease | plummer vinson syndrome |
| Definition | A syndrome of DYSPHAGIA with IRON-DEFICIENCY ANEMIA that is due to congenital anomalies in the ESOPHAGUS (such as cervical esophageal webs). It is known as Patterson-Kelly syndrome in the United Kingdom. |
| Synonym | anemia, plummer-vinson brown-kelly-paterson syndrome dysphagia, sideropenic kelly - paterson syndrome kelly syndrome kelly's syndrome kelly-paterson syndrome kellys syndrome paterson-brown-kelly syndrome paterson-kelly syndrome patterson brown kelly syndrome patterson kelly syndrome patterson syndrome patterson's syndrome patterson-brown-kelly syndrome patterson-kelly syndrome pattersons syndrome plummer - vinson syndrome plummer vinson anemia plummer-vinson syndr. plummer-vinson syndrome plummer-vinson syndrome (disorder) plummer-vinson syndrome [disease/finding] plummer-vinson-patterson-kelly syndrome sideropenic dysphagia syndrome, kelly's syndrome, patterson's syndrome, patterson-brown-kelly syndrome, patterson-kelly syndrome, plummer vinson syndrome, plummer-vinson |
| Orphanet | |
| OMIM | |
| ICD10 | |
| UMLS | C0032249 |
| MeSH | |
| SNOMED-CT | |
| Comorbidity | UMLS | Disease | Sentences' Count(Total Sentences:4) C0014859 | esophageal cancer | 1 C0010346 | crohn's disease | 1 C0007570 | coeliac disease | 1 C1527336 | sjogren's syndrome | 1 |
| Curated Gene | (Waiting for update.) |
| Inferring Gene | (Waiting for update.) |
| Text Mined Gene | (Waiting for update.) |
| Locus | (Waiting for update.) |
| Disease ID | 1754 |
|---|---|
| Disease | plummer vinson syndrome |
| Integrated Phenotype | (Waiting for update.) |
| Text Mined Phenotype | HPO | Name | Sentences' Count(Total Phenotypes:7) |
| Disease ID | 1754 |
|---|---|
| Disease | plummer vinson syndrome |
| Manually Symptom | (Waiting for update.) |
| 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) | |
|---|---|
| (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 | 1754 |
|---|---|
| Disease | plummer vinson syndrome |
| Case | (Waiting for update.) |