About: Familial Atypical Mole Melanoma Syndrome     Goto   Sponge   NotDistinct   Permalink

An Entity of Type : owl:Class, within Data Space : linked.opendata.cz:8890 associated with source document(s)

AttributesValues
rdf:type
rdfs:label
  • Familial Atypical Mole Melanoma Syndrome
rdfs:subClassOf
equivalentClass
Semantic_Type
  • Neoplastic Process
Preferred_Name
  • Familial Atypical Mole Melanoma Syndrome
UMLS_CUI
  • C2314896
ALT_DEFINITION
  • An inherited condition marked by the following: (1) one or more first- or second-degree relatives (parent, sibling, child, grandparent, grandchild, aunt, or uncle) with malignant melanoma; (2) many moles, some of which are atypical (asymmetrical, raised, and/or different shades of tan, brown, black, or red) and often of different sizes; and (3) moles that have specific features when examined under a microscope. FAMMM syndrome increases the risk of melanoma and may increase the risk of pancreatic cancer.NCI-GLOSS
Neoplastic_Status
  • Undetermined
Legacy_Concept_Name
  • Familial_Atypical_Mole_Melanoma_Syndrome
FULL_SYN
  • familial atypical multiple mole melanoma syndromePTNCI-GLOSSCDR0000270857
  • FAMM SyndromeSYNCI
  • FAMMM syndromePTNCI-GLOSSCDR0000270858
  • Familial Atypical Mole Melanoma SyndromePTNCI
DEFINITION
  • An autosomal dominant hereditary neoplastic syndrome characterized by the presence of multiple melanocytic nevi, some of which are atypical, and a family history of melanoma. Patients are at an increased risk of developing melanoma and pancreatic cancer.NCI
code
  • C27264
is someValuesFrom of
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