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
Displaying entries 21 - 30 of 37 in total
Gene ID Gene Symbol Description Source
4507 MTAP methylthioadenosine phosphorylase
5290 PIK3CA phosphatidylinositol-4,5-bisphosphate 3-kinase catalytic subunit alpha
5319 PLA2G1B phospholipase A2 group IB
5320 PLA2G2A phospholipase A2 group IIA
5728 PTEN phosphatase and tensin homolog
5743 PTGS2 prostaglandin-endoperoxide synthase 2
6383 SDC2 syndecan 2
7412 VCAM1 vascular cell adhesion molecule 1
8434 RECK reversion inducing cysteine rich protein with kazal motifs
8692 HYAL2 hyaluronidase 2

About Release Notes Help Feedback

Click here to visit the beta site.


International Collaboration

GlyCosmos is a member of the GlySpace Alliance together with GlyGen and Glycomics@ExPASy.

Acknowledgements

Supported by JST NBDC Grant Number JPMJND2204

Partly supported by NIH Common Fund Grant #1U01GM125267-01


Logo License Policies Site Map

Contact: support@glycosmos.org

This work is licensed under Creative Commons Attribution 4.0 International


GlyCosmos Portal v4.0.0

Last updated: August 19, 2024