Human Phenotype Ontology 
Grandparent Node:
expandAbnormality of the face (HP:0000271)help
Parent Node:
expandAbnormality of muscle of facial expression (HP:0430019)help
Parent Node:
expandAbnormality of the chin (HP:0000306)help
..Starting node
..expandAbnormality of mentalis muscle (HP:3000007)help
Term ID: 3000007
Name: Abnormality of mentalis muscle
Synonym:
Definition: An abnormality of a mentalis muscle.
Comments:
Reference: HP:3000007
Genes and Diseases:
 
       Child Nodes:

 Sister Nodes: 
..expandAbnormality of depressor labii inferioris (HP:3000029) help
..expandBroad chin (HP:0011822) help
..expandChin with H-shaped crease (HP:0011824) help
..expandChin with horizontal crease (HP:0011823) help
..expandChin with vertical crease (HP:0400001) 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:3000007HP:3000007Abnormality of mentalis muscle0 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.