Human Phenotype Ontology 
Grandparent Node:
expandAbnormal peripheral nervous system morphology (HP:0000759)help
Parent Node:
expandAbnormal cranial nerve morphology (HP:0001291)help
..Starting node
..expandCranial nerve motor loss (HP:0007097)help
Term ID: 7097
Name: Cranial nerve motor loss
Synonym:
Definition:
Comments:
Reference: HP:0007097
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 eleventh cranial nerve (HP:0010825) 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 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:0007097HP:0007097Cranial nerve motor loss0SLC52A3 CL E G H11327816187OMIM:211530Brown-Vialetto-Van laere syndrome 1.51


Genes (1) :SLC52A3

Diseases (1) :OMIM:211530
 

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