Human Phenotype Ontology 
Grandparent Node:
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Abnormality of the nervous system (HP:0000707)help
Parent Node:
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Abnormality of ganglion (HP:0410014)help
..Starting node
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Abnormality of cranial ganglion (HP:0410016)help
Term ID: 410016
Name: Abnormality of cranial ganglion
Synonym:
Definition: An abnormality of nerve cell cluster or a group of nerve cell bodies located in the autonomic nervous system of the cranium.
Comments:
Reference: HP:0410016
Genes and Diseases:
 
       Child Nodes:
........expandAbnormality of ciliary ganglion (HP:3000025) help

 Sister Nodes: 
..expandAbnormality of ganglion of peripheral nervous system (HP:0410015) 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:0410016HP:0410016Abnormality of cranial ganglion0 CL E G H
HP:0410016HP:3000025Abnormality of ciliary ganglion1 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.