Human Phenotype Ontology 
Grandparent Node:
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Melanoma (HP:0002861)help
Grandparent Node:
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Neoplasm of the skin (HP:0008069)help
Parent Node:
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Cutaneous melanoma (HP:0012056)help
..Starting node
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Lentigo maligna melanoma (HP:0012059)help
Term ID: 12059
Name: Lentigo maligna melanoma
Synonym:
Definition: A subtype of melanoma in situ that typically develops on sun-damaged skin. The lesion is typically a large, irregularly pigmented macule that has developed from an ordinary lentigo (a small pigmented spot on the skin with a clearly-defined edge). Change to a malignant lentigo typically takes place over 20 years or more, and many patients accept the change as a consequence of aging.
Comments:
Reference: HP:0012059
Genes and Diseases:
 
       Child Nodes:

 Sister Nodes: 
..expandAcral lentiginous melanoma (HP:0012060) help
..expandNodular melanoma (HP:0012058) help
..expandSuperficial spreading melanoma (HP:0012057) help
InputHPO IDHPO termDistanceGeneGene id entrezHGNC IDDiseaseIdDiseaseNameFrequencyOnsetHGMD variantsClinVar variants
 
HPO disease - gene - phenotype typical associations:
 
HPO disease - gene - phenotype less frequent non-typical associations:
HP:0012059HP:0012059Lentigo maligna melanoma0BRAF CL E G H6731097OMIM:613706Noonan syndrome 7276


Genes (1) :BRAF

Diseases (1) :OMIM:613706
 

Human Phenotype Ontology(HPO) is developed by the Human Phenotype Ontology Consortium. The version used here is December 15 2022 release.