PedAM
Pediatric Disease Annotations & Medicines
| scleredema | ||||
| Disease ID | 771 |
|---|---|
| Disease | scleredema |
| Definition | A diffuse, non-pitting induration of the skin of unknown etiology that occurs most commonly in association with diabetes mellitus, predominantly in females. It typically begins on the face or head and spreads to other areas of the body, sometimes involving noncutaneous tissues. Often it is preceded by any of various infections, notably staphylococcal infections. The condition resolves spontaneously, usually within two years of onset. (From Dorland, 27th ed) |
| Synonym | buschke scleredema buschke scleredema adultorum buschke scleredema diabeticorum buschke's scleredema buschkes scleredema diabeticorum, scleredema diabeticorums, scleredema scleredema (disorder) scleredema -retired- scleredema adultorum scleredema adultorum [disease/finding] scleredema adultorum of buschke scleredema diabeticorum scleredema diabeticorum of buschke scleredema diabeticorums scleredema, buschke's scleredemas scleroedema |
| Orphanet | |
| DOID | |
| UMLS | C0036413 |
| MeSH | |
| SNOMED-CT | |
| Comorbidity | UMLS | Disease | Sentences' Count(Total Sentences:9) C0011847 | diabetes | 1 C0034735 | raynaud's phenomenon | 1 C0026764 | myeloma | 1 C0011860 | type 2 diabetes | 1 C0011860 | type 2 diabetes mellitus | 1 C0030489 | paraproteinemia | 1 C0011849 | diabetes mellitus | 1 C1527336 | sjogren's syndrome | 1 C0023787 | lipodystrophy | 1 |
| Curated Gene | (Waiting for update.) |
| Inferring Gene | (Waiting for update.) |
| Text Mined Gene | Entrez_id | Symbol | Score | Resource(Total Genes:6) |
| Locus | (Waiting for update.) |
| Disease ID | 771 |
|---|---|
| Disease | scleredema |
| Integrated Phenotype | (Waiting for update.) |
| Text Mined Phenotype | HPO | Name | Sentences' Count(Total Phenotypes:4) HP:0030880 | Raynaud phenomenon | 1 HP:0000819 | Diabetes mellitus | 1 HP:0011838 | Sclerodactyly | 1 HP:0009125 | Lipodystrophy | 1 |
| Disease ID | 771 |
|---|---|
| Disease | scleredema |
| Manually Symptom | UMLS | Name(Total Manually Symptoms:4) |
| Text Mined Symptom | UMLS | Name | Sentences' Count(Total Symptoms:1) |
Manually Genotype(Total Text Mining Genotypes:0) |
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| (Waiting for update.) |
All Snps(Total Genotypes:0) | |
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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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Chemical(Total Drugs:0) | |
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| (Waiting for update.) | |
FDA approved drug and dosage information(Total Drugs:0) | |
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FDA labeling changes(Total Drugs:0) | |
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