spiradenoma |
Disease ID | 1390 |
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Disease | spiradenoma |
Definition | A benign epithelial neoplasm with eccrine or apocrine differentiation, arising from the sweat glands. It usually presents as a solitary, well circumscribed, firm nodule in the face and upper trunk. It is characterized by the presence of basaloid cells forming nodules in the dermis. Cases of carcinoma arising from long standing spiradenomas have been reported. |
Synonym | benign eccrine spiradenoma eccrine spiradenoma eccrine spiradenoma (morphologic abnormality) eccrine spiradenoma of skin eccrine spiradenoma of skin (disorder) spiradenoma eccrine spiradenoma, nos spiradenomas |
DOID | |
UMLS | C0334347 |
SNOMED-CT | |
Comorbidity | UMLS | Disease | Sentences' Count(Total Sentences:1) |
Curated Gene | (Waiting for update.) |
Inferring Gene | (Waiting for update.) |
Text Mined Gene | Entrez_id | Symbol | Score | Resource(Total Genes:37) 3861 | KRT14 | DISEASES 6449 | SGTA | DISEASES 1048 | CEACAM5 | DISEASES 4254 | KITLG | DISEASES 3852 | KRT5 | DISEASES 3866 | KRT15 | DISEASES 1022 | CDK7 | DISEASES 999 | CDH1 | DISEASES 8312 | AXIN1 | DISEASES 22822 | PHLDA1 | DISEASES 7157 | TP53 | DISEASES 3858 | KRT10 | DISEASES 27123 | DKK2 | DISEASES 231 | AKR1B1 | DISEASES 3815 | KIT | DISEASES 5304 | PIP | DISEASES 563 | AZGP1 | DISEASES 3856 | KRT8 | DISEASES 117159 | DCD | DISEASES 10630 | PDPN | DISEASES 171558 | PTCRA | DISEASES 1540 | CYLD | DISEASES 2932 | GSK3B | DISEASES 3855 | KRT7 | DISEASES 1538 | CYLC1 | DISEASES 1364 | CLDN4 | DISEASES 1499 | CTNNB1 | DISEASES 55107 | ANO1 | DISEASES 4311 | MME | DISEASES 6663 | SOX10 | DISEASES 7042 | TGFB2 | DISEASES 10763 | NES | DISEASES 7046 | TGFBR1 | DISEASES 3875 | KRT18 | DISEASES 387836 | CLEC2A | DISEASES 2939 | GSTA2 | DISEASES 4345 | CD200 | DISEASES |
Locus | (Waiting for update.) |
Disease ID | 1390 |
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Disease | spiradenoma |
Integrated Phenotype | (Waiting for update.) |
Text Mined Phenotype | HPO | Name | Sentences' Count(Total Phenotypes:3) |
Disease ID | 1390 |
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Disease | spiradenoma |
Manually Symptom | UMLS | Name(Total Manually Symptoms:1) C1608408 | malignant transformation |
Text Mined Symptom | (Waiting for update.) |
Manually Genotype(Total Text Mining 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.) |
Chemical(Total Drugs:0) | |
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(Waiting for update.) |
FDA approved drug and dosage information(Total Drugs:0) | |
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(Waiting for update.) |
FDA labeling changes(Total Drugs:0) | |
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(Waiting for update.) |