Human Phenotype Ontology 
Grandparent Node:
expandAbnormal oral morphology (HP:0031816)help
Parent Node:
expandAbnormal oral cavity morphology (HP:0000163)help
..Starting node
..expandAbnormal mouth floor morphology (HP:0410012)help
Term ID: 410012
Name: Abnormal mouth floor morphology
Synonym: Abnormality of the floor of mouth; Abnormality of the mouth floor
Definition: Any abnormality of the mouth floor.
Comments:
Reference: HP:0410012
Genes and Diseases:
 
       Child Nodes:
........expandAbnormality of mylohyoid muscle (HP:3000008) help

 Sister Nodes: 
..expandAbnormal lip morphology (HP:0000159) help
..expandAbnormal mandibular ramus morphology (HP:3000003) help
..expandAbnormal oral frenulum morphology (HP:0000190) help
..expandAbnormal oral mucosa morphology (HP:0011830) help
..expandAbnormal palate morphology (HP:0000174) help
..expandAbnormal salivary gland morphology (HP:0010286) help
..expandAbnormality of mouth shape (HP:0011338) help
..expandAbnormality of mouth size (HP:0011337) help
..expandAbnormality of the alveolar ridges (HP:0006477) help
..expandAbnormality of the dentition (HP:0000164) help
..expandAbnormality of the tongue (HP:0000157) help
..expandNeoplasm of the oral cavity (HP:0100649) 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:0410012HP:0410012Abnormal mouth floor morphology0 CL E G H
HP:0410012HP: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.