Human Phenotype Ontology 
Grandparent Node:
expand
Hyperpigmentation of the skin (HP:0000953)help
Parent Node:
expand
Abnormal lip morphology (HP:0000159)help
Parent Node:
expand
Irregular hyperpigmentation (HP:0007400)help
..Starting node
..expand
Lip hyperpigmentation (HP:0100816)help
Term ID: 100816
Name: Lip hyperpigmentation
Synonym: Darkening of skin of the lips; Hyperpigmentation of lip vermillion; Increased pigmentation on the lips
Definition:
Comments:
Reference: HP:0100816
Genes and Diseases:
 
       Child Nodes:

 Sister Nodes: 
..expandForehead hyperpigmentation (HP:0005336) help
..expandHypermelanotic macule (HP:0001034) help
..expandHyperpigmentation of eyelids (HP:0007406) help
..expandHyperpigmented streaks (HP:0007572) help
..expandIncreased groin pigmentation with raindrop depigmentation (HP:0007450) help
..expandIrregular hyperpigmentation of back (HP:0007521) help
..expandLinear hyperpigmentation (HP:0007546) help
..expandProgressive reticulate hyperpigmentation (HP:0007456) help
..expandReticular hyperpigmentation (HP:0007588) help
..expandSpotty hyperpigmentation (HP:0005585) 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:0100816HP:0100816Lip hyperpigmentation0ABCD1 CL E G H21561ORPHA:139399AdrenomyeloneuropathyHP:0040282 - Frequent135


Genes (1) :ABCD1

Diseases (1) :ORPHA:139399
 

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