Human Phenotype Ontology 
Grandparent Node:
expand
Abnormal soft palate morphology (HP:0100736)help
Grandparent Node:
expand
Abnormality of the musculature (HP:0003011)help
Parent Node:
expand
Abnormality of extrinsic muscle of tongue (HP:0040174)help
Parent Node:
expand
Abnormality of musculature of soft palate (HP:0430014)help
..Starting node
..expand
Abnormality of palatoglossus muscle (HP:3000011)help
Term ID: 3000011
Name: Abnormality of palatoglossus muscle
Synonym:
Definition: An abnormality of a palatoglossus muscle.
Comments:
Reference: HP:3000011
Genes and Diseases:
 
       Child Nodes:

 Sister Nodes: 
..expandAbnormality of levator veli palatini muscle (HP:3000073) help
..expandAbnormality of palatopharyngeus muscle (HP:3000012) help
..expandAbnormality of tensor veli palatini muscle (HP:0430016) help
..expandAbnormality of uvular muscle (HP:0430017) 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:3000011HP:3000011Abnormality of palatoglossus 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.