Human Phenotype Ontology 
Grandparent Node:
expandAbnormality of facial soft tissue (HP:0011799)help
Grandparent Node:
expandAbnormality of the musculature (HP:0003011)help
Parent Node:
expandAbnormality of facial musculature (HP:0000301)help
..Starting node
..expandAbnormality of nasal musculature (HP:0430018)help
Term ID: 430018
Name: Abnormality of nasal musculature
Synonym: Abnormality of muscle of nose; Abnormality of musculature of the nose; Abnormality of nasal musculature
Definition: An abnormality of the muscles of the structure of the nose.
Comments:
Reference: HP:0430018
Genes and Diseases:
 
       Child Nodes:
........expandAbnormality of nasalis muscle (HP:3000009) help
........expandAbnormality of procerus muscle (HP:3000014) help

 Sister Nodes: 
..expandAbnormal platysma muscle morphology (HP:3000013) help
..expandAbnormality of jaw muscles (HP:0045037) help
..expandAbnormality of muscle of facial expression (HP:0430019) help
..expandAbnormality of mylohyoid muscle (HP:3000008) help
..expandFacial hypotonia (HP:0000297) help
..expandFacial muscle hypertrophy (HP:0012892) help
..expandFacial myokymia (HP:0000317) help
..expandHypomimic face (HP:0000338) help
..expandHypoplasia of facial musculature (HP:0004660) help
..expandSpasticity of facial muscles (HP:0002491) help
..expandWeakness of facial musculature (HP:0030319) 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:0430018HP:0430018Abnormality of nasal musculature0 CL E G H
HP:0430018HP:3000009Abnormality of nasalis muscle1 CL E G H
HP:0430018HP:3000014Abnormality of procerus 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.