Human Phenotype Ontology 
Grandparent Node:
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Vocal cord paralysis (HP:0001605)help
Parent Node:
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Vocal cord paresis (HP:0001604)help
..Starting node
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Bilateral vocal cord paresis (HP:0012822)help
Term ID: 12822
Name: Bilateral vocal cord paresis
Synonym:
Definition: Decreased strength of the vocal fold on both sides.
Comments:
Reference: HP:0012822
Genes and Diseases:
 
       Child Nodes:

 Sister Nodes: 
..expandUnilateral vocal cord paresis (HP:0012821) 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:0012822HP:0012822Bilateral vocal cord paresis0DST CL E G H6671090OMIM:614653Neuropathy, hereditary sensory and autonomic, type VI108


Genes (1) :DST

Diseases (1) :OMIM:614653
 

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