Melanocytic Nevus Syndrome, Congenital (CMNS)

Alias:
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
Related ID:

Basic Information

Inheritance
Age of Onset
Prevalence
Related Gene
Related Mouse Models
Reference
MALACARDS
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Unknown
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3
41
22

Medical Symptom

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Categorization
Description
HPO Frequency
Orphanet Frequency
HPO Source Accession
No data available

Gene & Mutation

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Gene
Function
Score
Mutations
No data available

Related Drugs

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CAS Number
Status
Phase
No data available

Disease Model

Category
Name
MGI
Related Gene
Strain of Origin
Publications
No data available

References Literature

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PMID
Journal
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IF
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