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 1 - 10 of 37 in total
Gene ID Gene Symbol Description Source
48 ACO1 aconitase 1
142 PARP1 poly(ADP-ribose) polymerase 1
250 ALPP alkaline phosphatase, placental
960 CD44 CD44 molecule (IN blood group)
1298 COL9A2 collagen type IX alpha 2 chain
1464 CSPG4 chondroitin sulfate proteoglycan 4
1545 CYP1B1 cytochrome P450 family 1 subfamily B member 1
1589 CYP21A2 cytochrome P450 family 21 subfamily A member 2
1594 CYP27B1 cytochrome P450 family 27 subfamily B member 1
2194 FASN fatty acid synthase

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