Human Phenotype Ontology 
Grandparent Node:
expandAbnormality of the head (HP:0000234)help
Parent Node:
expandAbnormality of the face (HP:0000271)help
..Starting node
..expandAbnormality of the submandibular region (HP:0410013)help
Term ID: 410013
Name: Abnormality of the submandibular region
Synonym:
Definition: Any abnormality of the submandibular region, the region between the mandible and the hyoid bone contains the submandibular and sublingual glands, suprahyoid muscles, submandibular ganglion, and lingual artery.
Comments:
Reference: HP:0410013
Genes and Diseases:
 
       Child Nodes:
........expandAbnormality of mylohyoid muscle (HP:3000008) help

 Sister Nodes: 
..expandAbnormal facial expression (HP:0005346) help
..expandAbnormal facial shape (HP:0001999) help
..expandAbnormal midface morphology (HP:0000309) help
..expandAbnormality of facial soft tissue (HP:0011799) help
..expandAbnormality of the chin (HP:0000306) help
..expandAbnormality of the forehead (HP:0000290) help
..expandAbnormality of the mouth (HP:0000153) help
..expandAbnormality of the nose (HP:0000366) help
..expandAbnormality of the orbital region (HP:0000315) help
..expandAbnormality of the periorbital region (HP:0000606) help
..expandCraniofacial dysostosis (HP:0004439) help
..expandCraniofacial hyperostosis (HP:0004493) help
..expandFacial cleft (HP:0002006) 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:0410013HP:0410013Abnormality of the submandibular region0 CL E G H
HP:0410013HP:3000008Abnormality of mylohyoid muscle1 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.