| elastosis perforans serpiginosa | ||||
| Disease ID | 1160 |
|---|---|
| Disease | elastosis perforans serpiginosa |
| Definition | Elastosis perforans serpiginosa is a unique perforating disorder characterized by transepidermal elimination of elastic fibers and distinctive clinical lesions, which are serpiginous in distribution and can be associated with specific diseases.[1][2] - Wikipedia Reference: https://en.wikipedia.org/wiki/elastosis perforans serpiginosa |
| Synonym | elastoma intrapapillare perforans verruciformis elastosis perforans elastosis perforans serpiginosa (disorder) keratosis follicularis serpiginosa lutz-miescher disease miescher elastoma miescher's elastoma perforating elastoma perforating elastosis perforating serpiginous elastosis |
| Orphanet | |
| OMIM | |
| ICD10 | |
| UMLS | C0221271 |
| SNOMED-CT | |
| Comorbidity | UMLS | Disease | Sentences' Count(Total Sentences:2) |
| Curated Gene | (Waiting for update.) |
| Inferring Gene | (Waiting for update.) |
| Text Mined Gene | (Waiting for update.) |
| Locus | (Waiting for update.) |
| Disease ID | 1160 |
|---|---|
| Disease | elastosis perforans serpiginosa |
| Integrated Phenotype | HPO | Name(Total Integrated Phenotypes:1) HP:0003764 | Naevus |
| Text Mined Phenotype | (Waiting for update.) |
| Disease ID | 1160 |
|---|---|
| Disease | elastosis perforans serpiginosa |
| Manually Symptom | UMLS | Name(Total Manually Symptoms:1) C0003496 | aortic rupture |
| Text Mined Symptom | (Waiting for update.) |
Manually Genotype(Total Text Mining Genotypes:0) |
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All Snps(Total Genotypes:0) | |
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GWASdb Annotation(Total Genotypes:0) | |
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Mapped by lexical matching(Total Items:0) |
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Mapped by homologous gene(Total Items:0) |
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Chemical(Total Drugs:0) | |
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FDA approved drug and dosage information(Total Drugs:0) | |
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FDA labeling changes(Total Drugs:0) | |
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