Human Phenotype Ontology 
Grandparent Node:
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Abnormality of the face (HP:0000271)help
Parent Node:
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Abnormality of muscle of facial expression (HP:0430019)help
Parent Node:
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Abnormality of the chin (HP:0000306)help
..Starting node
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Abnormality of depressor labii inferioris (HP:3000029)help
Term ID: 3000029
Name: Abnormality of depressor labii inferioris
Synonym: Abnormality of depressor labii inferioris muscle
Definition: An abnormality of a depressor labii inferioris.
Comments:
Reference: HP:3000029
Genes and Diseases:
 
       Child Nodes:

 Sister Nodes: 
..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
..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:3000029HP:3000029Abnormality of depressor labii inferioris0 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.