Human Phenotype Ontology 
Grandparent Node:
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Abnormality of the face (HP:0000271)help
Parent Node:
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Abnormality of nasal musculature (HP:0430018)help
Parent Node:
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Abnormality of the nose (HP:0000366)help
..Starting node
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Abnormality of procerus muscle (HP:3000014)help
Term ID: 3000014
Name: Abnormality of procerus muscle
Synonym:
Definition: An abnormality of a procerus.
Comments:
Reference: HP:3000014
Genes and Diseases:
 
       Child Nodes:

 Sister Nodes: 
..expandAbnormal external nose morphology (HP:0010938) help
..expandAbnormal nasal base norphology (HP:0012808) help
..expandAbnormal nasal bridge morphology (HP:0000422) help
..expandAbnormal nasal morphology (HP:0005105) help
..expandAbnormal nasal mucosa morphology (HP:0000433) help
..expandAbnormal nasal septum morphology (HP:0000419) help
..expandAbnormal nasal skeleton morphology (HP:0010937) help
..expandAbnormal nasopharynx morphology (HP:0001739) help
..expandAbnormal nostril morphology (HP:0005288) help
..expandAbnormality of nasal hair (HP:0040057) help
..expandAbnormality of nasalis muscle (HP:3000009) help
..expandAbnormality of the choanae (HP:0000415) help
..expandAbnormality of the nasal cavity (HP:0010640) help
..expandAbnormality of the nasolabial region (HP:0005289) help
..expandAbnormality of the sense of smell (HP:0004408) help
..expandEpistaxis (HP:0000421) help
..expandNasal congestion (HP:0001742) help
..expandRhinitis (HP:0012384) 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:3000014HP:3000014Abnormality of procerus 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.