eRAM
encyclopedia of Rare Disease Annotation for Precision Medicine
| degos disease | ||||
| Disease ID | 1259 |
|---|---|
| Disease | degos disease |
| Definition | Variously described as a vasculopathy, endovasculitis, or occlusive arteriopathy, this condition occurs in a benign cutaneous form and a lethal multiorgan systemic variant. It is characterized by a narrowing and occlusion of the lumen of small to medium-sized blood vessels, leading to ischemia and infarction in the involved organ systems. The etiology and pathophysiology are unknown. |
| Synonym | atrophic papuloses, malignant atrophic papulosis, malignant cutaneointestinal syndrome degos syndrome degos' disease degos's malignant atrophic papulosis disease, degos disease, kohlmeier-degos erythrokeratoderma en cocarde (degos) erythrokeratoderma en cocardes erythrokeratoderma en cocardes (degos syndrome) erythrokeratoderma en cocardes (disorder) koehlmeier-degos syndrome kohlmeier-degos disease kohlmeier-degos syndrome lethal cutaneous and gastrointestinal arteriolar thrombosis maladie de degos malignant atrophic papuloses malignant atrophic papulosis malignant atrophic papulosis (disorder) malignant atrophic papulosis [disease/finding] malignant atrophic papulosis of degos map - malignant atrophic papulosis papuloses, malignant atrophic papulosis, malignant atrophic papulosis, malignant, atrophic syndrome, degos |
| Orphanet | |
| OMIM | |
| UMLS | C0221011 |
| MeSH | |
| SNOMED-CT | |
| Comorbidity | UMLS | Disease | Sentences' Count(Total Sentences:6) C0021845 | intestinal perforation | 3 C0004943 | behcet's disease | 1 C0162836 | hidradenitis suppurativa | 1 C0085160 | hidradenitis | 1 C0011633 | dermatomyositis | 1 C0155765 | microangiopathy | 1 |
| Curated Gene | (Waiting for update.) |
| Inferring Gene | (Waiting for update.) |
| Text Mined Gene | (Waiting for update.) |
| Locus | (Waiting for update.) |
| Disease ID | 1259 |
|---|---|
| Disease | degos disease |
| Integrated Phenotype | (Waiting for update.) |
| Text Mined Phenotype | HPO | Name | Sentences' Count(Total Phenotypes:3) |
| Disease ID | 1259 |
|---|---|
| Disease | degos disease |
| Manually Symptom | UMLS | Name(Total Manually Symptoms:1) C0858617 | posterior subcapsular cataract |
| Text Mined Symptom | (Waiting for update.) |
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 | 1259 |
|---|---|
| Disease | degos disease |
| Case | (Waiting for update.) |