Human Phenotype Ontology 
Grandparent Node:
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Abnormality of facial musculature (HP:0000301)help
Parent Node:
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Abnormality of muscle of facial expression (HP:0430019)help
..Starting node
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Abnormality of depressor anguli oris muscle (HP:3000028)help
Term ID: 3000028
Name: Abnormality of depressor anguli oris muscle
Synonym:
Definition: An abnormality of a depressor anguli oris muscle.
Comments:
Reference: HP:3000028
Genes and Diseases:
 
       Child Nodes:

 Sister Nodes: 
..expandAbnormality of depressor labii inferioris (HP:3000029) help
..expandAbnormality of levator anguli oris (HP:3000070) help
..expandAbnormality of levator labii superioris (HP:3000071) help
..expandAbnormality of levator labii superioris alaeque nasi muscle (HP:0430020) help
..expandAbnormality of mentalis muscle (HP:3000007) help
..expandAbnormality of orbicularis oris muscle (HP:3000010) help
..expandAbnormality of risorius muscle (HP:3000015) help
..expandAbnormality of zygomaticus major muscle (HP:3000018) help
..expandAbnormality of zygomaticus minor muscle (HP:3000020) 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:3000028HP:3000028Abnormality of depressor anguli oris 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.