Human Phenotype Ontology 
Grandparent Node:
Abnormality of head or neck (HP:0000152)help
Parent Node:
Abnormal cranial nerve morphology (HP:0001291)help
Parent Node:
Abnormality of peripheral nerves (HP:0045010)help
Parent Node:
Abnormality of the head (HP:0000234)help
..Starting node
Abnormal glossopharyngeal nerve morphology (HP:3000047)help
Term ID: 3000047
Name: Abnormal glossopharyngeal nerve morphology
Synonym: Abnormality of glossopharyngeal nerve
Definition: Any structural anomaly of the glossopharyngeal nerve, the ninth paired cranial nerve (CN IX).
Reference: HP:3000047
Genes and Diseases:
       Child Nodes:

 Sister Nodes: 
..expandAbnormal great auricular nerve morphology (HP:3000048) help
..expandAbnormal head blood vessel morphology (HP:3000036) help
..expandAbnormal lingual nerve morphology (HP:3000075) help
..expandAbnormal scalp morphology (HP:0001965) help
..expandAbnormal skull morphology (HP:0000929) help
..expandAbnormality of inferior alveolar nerve (HP:3000055) help
..expandAbnormality of infra-orbital nerve (HP:3000061) help
..expandAbnormality of occipitofrontalis muscle (HP:0040172) help
..expandAbnormality of the face (HP:0000271) help
..expandAbnormality of the pharynx (HP:0000600) help
..expandFixed head retroflexion (HP:0031178) 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:3000047HP:3000047Abnormal glossopharyngeal nerve morphology0 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.