Human Phenotype Ontology 
Grandparent Node:
expandInvoluntary movements (HP:0004305)help
Parent Node:
expandMyoclonus (HP:0001336)help
..Starting node
..expandPalatal tremor (HP:0010530)help
Term ID: 10530
Name: Palatal tremor
Synonym: Palatal myoclonus
Definition: Palatal tremor (PT) is an involuntary, rhythmic and oscillatory movement of the soft palate. PT is a rare type of tremor involving the soft palate. It can be unilateral or bilateral.
Comments:
Reference: HP:0010530
Genes and Diseases:
 
       Child Nodes:

 Sister Nodes: 
..expandChin myoclonus (HP:0012462) help
..expandCortical myoclonus (HP:0040148) help
..expandErratic myoclonus (HP:0025357) help
..expandEyelid myoclonus (HP:0025097) help
..expandLimb myoclonus (HP:0045084) help
..expandMorning myoclonic jerks (HP:0007000) help
..expandMyoclonic spasms (HP:0003739) help
..expandSleep myoclonus (HP:0012323) help
..expandSpinal myoclonus (HP:0010531) 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:0010530HP:0010530Palatal tremor0CYP27A1 CL E G H15932605ORPHA:909Cerebrotendinous xanthomatosisHP:0040284 - Very rare114
HP:0010530HP:0010530Palatal tremor0FTL CL E G H25123999ORPHA:157846NeuroferritinopathyHP:0040283 - Occasional33
HP:0010530HP:0010530Palatal tremor0GFAP CL E G H26704235OMIM:203450Alexander disease188
HP:0010530HP:0010530Palatal tremor0GFAP CL E G H26704235ORPHA:363717Alexander disease type I188
HP:0010530HP:0010530Palatal tremor0GFAP CL E G H26704235ORPHA:363722Alexander disease type II188


Genes (3) :CYP27A1 FTL GFAP

Diseases (5) :ORPHA:909 ORPHA:157846 OMIM:203450 ORPHA:363717 ORPHA:363722
 

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