Human Phenotype Ontology 
Grandparent Node:
Hyperpigmentation of the skin (HP:0000953)help
Grandparent Node:
Hypopigmentation of the skin (HP:0001010)help
Parent Node:
Mixed hypo- and hyperpigmentation of the skin (HP:0009123)help
..Starting node
Axillary and groin hyperpigmentation and hypopigmentation (HP:0007471)help
Term ID: 7471
Name: Axillary and groin hyperpigmentation and hypopigmentation
Reference: HP:0007471
Genes and Diseases:
       Child Nodes:

 Sister Nodes: 
..expandAreas of hypopigmentation and hyperpigmentation that do not follow Blaschko lines (HP:0007402) help
..expandHyperpigmented/hypopigmented macules (HP:0007441) help
..expandIncreased groin pigmentation with raindrop depigmentation (HP:0007450) help
..expandPatchy hypo- and hyperpigmentation (HP:0007509) 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:0007471HP:0007471Axillary and groin hyperpigmentation and hypopigmentation0 CL E G H

Genes (0) :

Diseases (0) :

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