Human Phenotype Ontology 
Grandparent Node:
expandHyperpigmentation of the skin (HP:0000953)help
Parent Node:
expandAbnormality of the forehead (HP:0000290)help
Parent Node:
expandIrregular hyperpigmentation (HP:0007400)help
..Starting node
..expandForehead hyperpigmentation (HP:0005336)help
Term ID: 5336
Name: Forehead hyperpigmentation
Synonym: Darkening of the forehead
Definition:
Comments:
Reference: HP:0005336
Genes and Diseases:
 
       Child Nodes:

 Sister Nodes: 
..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
..expandLip hyperpigmentation (HP:0100816) 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:0005336HP:0005336Forehead hyperpigmentation0SEC23A CL E G H1048410701OMIM:607812Craniolenticulosutural dysplasia.2


Genes (1) :SEC23A

Diseases (1) :OMIM:607812
 

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