Melanocytic Nevus Syndrome, Congenital (CMNS)

Melanocytic Nevus Syndrome, Congenital(来自ICD-11)

别称:

Giant Pigmented Hairy Nevus

Epithelioid and Spindle Cell Nevus

Giant Congenital Pigmented Nevus

Congenital Melanocytic Nevus

Pigmented Moles

Nevus Spilus

Cmns

Gphn

Nevus Syndrome, Melanocytic, Congenital, Somatic

Melanocytic Nevus Syndrome, Congenital, Somatic

Spitz Nevus or Nevus Spilus, Somatic

Nevus, Spindle Cell and Epithelioid

Large Congenital Melanocytic Nevus

Spindle Cell and Epithelioid Nevus

Speckled Lentiginous Nevus

Melanocytic Nevus of Skin

Melanocytic Nevus

Nevoid Lentigo

Nevus, Spitz

Spitz Nevus

Nevuspi

Lentigo

Spitzn

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Basic Information

Medical Symptom

Gene & Mutation

Related Drugs

Disease Model

References Literature

Melanocytic Nevus Syndrome, Congenital, also known as giant pigmented hairy nevus, is related to spitzoid melanoma and nevus, epidermal. An important gene associated with Melanocytic Nevus Syndrome, Congenital is NRAS (NRAS Proto-Oncogene, GTPase), and among its related pathways/superpathways are Development EGFR signaling pathway and Development FGFR signaling pathway. The drugs Aminolevulinic acid and Glycolic acid have been mentioned in the context of this disorder. Affiliated tissues include skin and brain, and related phenotypes are hypertelorism and short nose

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