familial atypical multiple mole melanoma syndrome
50) and a family history of melanoma as well as, in a subset of patients, an increased risk of developing pancreatic cancer (see this term) and other malignancies
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familial atypical multiple mole melanoma syndrome
Summary
familial atypical multiple mole melanoma syndrome is a class of disease[1].
Key Facts
- familial atypical multiple mole melanoma syndrome's instance of is recorded as class of disease[2].
- familial atypical multiple mole melanoma syndrome's Orphanet ID is recorded as 404560[3].
- familial atypical multiple mole melanoma syndrome's genetic association is recorded as CDKN2A[4].
- familial atypical multiple mole melanoma syndrome's exact match is recorded as http://www.orpha.net/ORDO/Orphanet_404560[5].
- familial atypical multiple mole melanoma syndrome's UMLS CUI is recorded as C0013403[6].
- familial atypical multiple mole melanoma syndrome's UMLS CUI is recorded as C0205747[7].
- familial atypical multiple mole melanoma syndrome's UMLS CUI is recorded as C2314896[8].
- familial atypical multiple mole melanoma syndrome's UMLS CUI is recorded as C1838547[9].
- familial atypical multiple mole melanoma syndrome's ICD-10-CM is recorded as D22.9[10].
- familial atypical multiple mole melanoma syndrome's Mondo ID is recorded as MONDO_0018453[11].