Human Phenotype Ontology 
Grandparent Node:
expandAbnormality of the face (HP:0000271)help
Parent Node:
expandAbnormality of the chin (HP:0000306)help
..Starting node
..expandChin with vertical crease (HP:0400001)help
Term ID: 400001
Name: Chin with vertical crease
Synonym: Chin with vertical crease; Chin with vertical furrow; Chin with vertical groove; Chin with vertical sulcus; Chin, vertical crease; Cleft chin; Vertical chin skin cleft; Vertical menton crease
Definition: Vertical crease fold situated below the vermilion border of the lower lip and above the fatty pad of the chin with the face at rest.
Comments:
Reference: HP:0400001
Genes and Diseases:
 
       Child Nodes:

 Sister Nodes: 
..expandAbnormality of depressor labii inferioris (HP:3000029) help
..expandAbnormality of mentalis muscle (HP:3000007) help
..expandBroad chin (HP:0011822) help
..expandChin with H-shaped crease (HP:0011824) help
..expandChin with horizontal crease (HP:0011823) help
..expandCleft of chin (HP:0011323) help
..expandDimple chin (HP:0010751) help
..expandMandibular prognathia (HP:0000303) help
..expandPointed chin (HP:0000307) help
..expandShort chin (HP:0000331) help
..expandTall chin (HP:0400000) 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:0400001HP:0400001Chin with vertical crease0 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.