Human Phenotype Ontology 
Grandparent Node:
expandAbnormal peripheral nervous system morphology (HP:0000759)help
Parent Node:
expandAbnormal cranial nerve morphology (HP:0001291)help
..Starting node
..expandAbnormality of the eleventh cranial nerve (HP:0010825)help
Term ID: 10825
Name: Abnormality of the eleventh cranial nerve
Synonym: Abnormality of cranial nerve XI; Abnormality of the accessory nerve
Definition: Abnormality of the eleventh cranial nerve.
Comments:
Reference: HP:0010825
Genes and Diseases:
 
       Child Nodes:

 Sister Nodes: 
..expandAbnormal fifth cranial nerve morphology (HP:0010824) help
..expandAbnormal glossopharyngeal nerve morphology (HP:3000047) help
..expandAbnormal great auricular nerve morphology (HP:3000048) help
..expandAbnormal lingual nerve morphology (HP:3000075) help
..expandAbnormal sixth cranial nerve morphology (HP:0011348) help
..expandAbnormality of inferior alveolar nerve (HP:3000055) help
..expandAbnormality of infra-orbital nerve (HP:3000061) help
..expandAbnormality of the seventh cranial nerve (HP:0010827) help
..expandAbnormality of the vestibulocochlear nerve (HP:0009591) help
..expandCranial nerve compression (HP:0001293) help
..expandCranial nerve motor loss (HP:0007097) help
..expandCranial nerve paralysis (HP:0006824) help
..expandGustatory lacrimation (HP:0100274) help
..expandOculomotor nerve palsy (HP:0012246) 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:0010825HP:0010825Abnormality of the eleventh cranial nerve0DKK1 CL E G H229432891ORPHA:268882Arnold-Chiari malformation type IHP:0040282 - Frequent


Genes (1) :DKK1

Diseases (1) :ORPHA:268882
 

Human Phenotype Ontology(HPO) is developed by the Human Phenotype Ontology Consortium. The version used here is December 15 2022 release.