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dysplastic nevus syndrome
Summary
- Synonym
-
- FAMM syndrome
- familial atypical multiple mole-melanoma
- Definition
- A syndrome that is characterized by the presence of multiple dysplastic nevi (atypical moles) and a history of melanoma in two family members.
- Super Class
- autosomal dominant disease syndrome
External Links
- Disease Ontology
- DOID:10041
- Mondo Disease Ontology
- MeSH
- UMLS
- GARD
- MGI genotype (from TogoID)
Related Genes
| Gene ID | Gene Symbol | Description | Source |
|---|---|---|---|
| 2597 | GAPDH | glyceraldehyde-3-phosphate dehydrogenase | |
| 2923 | PDIA3 | protein disulfide isomerase family A member 3 | |
| 3251 | HPRT1 | hypoxanthine phosphoribosyltransferase 1 | |
| 3383 | ICAM1 | intercellular adhesion molecule 1 | |
| 3417 | IDH1 | isocitrate dehydrogenase (NADP(+)) 1 | |
| 3482 | IGF2R | insulin like growth factor 2 receptor | |
| 3956 | LGALS1 | galectin 1 | |
| 3958 | LGALS3 | galectin 3 | |
| 4241 | MELTF | melanotransferrin | |
| 4360 | MRC1 | mannose receptor C-type 1 |
Related Glycoprotein
