Human Phenotype Ontology 
Grandparent Node:
Reduced tendon reflexes (HP:0001315)help
Parent Node:
Abnormality of jaw muscles (HP:0045037)help
Parent Node:
Hyporeflexia (HP:0001265)help
..Starting node
Jaw hyporeflexia (HP:0012392)help
Term ID: 12392
Name: Jaw hyporeflexia
Synonym: Mandibular hyporeflexia
Definition: Reduced intensity of muscle tendon reflexes in jaw.
Reference: HP:0012392
Genes and Diseases:
       Child Nodes:

 Sister Nodes: 
..expandHyporeflexia of lower limbs (HP:0002600) help
..expandHyporeflexia of upper limbs (HP:0012391) 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:0012392HP:0012392Jaw hyporeflexia0 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.