Human Phenotype Ontology 
Grandparent Node:
expandMelanoma (HP:0002861)help
Grandparent Node:
expandNeoplasm of the skin (HP:0008069)help
Parent Node:
expandCutaneous melanoma (HP:0012056)help
..Starting node
..expandAcral lentiginous melanoma (HP:0012060)help
Term ID: 12060
Name: Acral lentiginous melanoma
Synonym:
Definition: A type of cutaneous melanoma localized to the palm, sole, or beneath the nail (subungual melanoma). Acral lentiginous melanoma starts as a slowly-enlarging flat patch of discoloured skin and usually displays a size above 6 mm and often several centimetres or more in diameter upon diagnosis and variable pigmentation with a mixutre of colors including brown, and blue-grey, black and red. The surface of the lesion is initially smooth but later in the course may become thicker and irregular, and may ulcerate or bleed.
Comments:
Reference: HP:0012060
Genes and Diseases:
 
       Child Nodes:

 Sister Nodes: 
..expandLentigo maligna melanoma (HP:0012059) 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:0012060HP:0012060Acral lentiginous melanoma0WRN CL E G H748612791ORPHA:902Werner syndromeHP:0040283 - Occasional310


Genes (1) :WRN

Diseases (1) :ORPHA:902
 

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