Human Phenotype Ontology 
Grandparent Node:
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Abnormal tongue physiology (HP:0030810)help
Parent Node:
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Movement abnormality of the tongue (HP:0000182)help
..Starting node
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Difficulty in tongue movements (HP:0000183)help
Term ID: 183
Name: Difficulty in tongue movements
Synonym: Difficulty in lingual movements; Difficulty in tongue movements; Hypokinesia of the tongue; Lingual hypokinesia
Definition:
Comments:
Reference: HP:0000183
Genes and Diseases:
 
       Child Nodes:

 Sister Nodes: 
InputHPO IDHPO termDistanceGeneGene id entrezHGNC IDDiseaseIdDiseaseNameFrequencyOnsetHGMD variantsClinVar variants
 
HPO disease - gene - phenotype typical associations:
 
HPO disease - gene - phenotype less frequent non-typical associations:
HP:0000183HP:0000183Difficulty in tongue movements0ALS2 CL E G H57679443OMIM:205100Amyotrophic lateral sclerosis 2, juvenile.114
HP:0000183HP:0000183Difficulty in tongue movements0ALS2 CL E G H57679443OMIM:606353Primary lateral sclerosis, juvenile.114
HP:0000183HP:0000183Difficulty in tongue movements0ATP13A2 CL E G H2340030213ORPHA:306674Kufor-Rakeb syndromeHP:0040282 - Frequent100
HP:0000183HP:0000183Difficulty in tongue movements0EDN1 CL E G H19063176ORPHA:137888Auriculocondylar syndromeHP:0040282 - Frequent6
HP:0000183HP:0000183Difficulty in tongue movements0FRAS1 CL E G H8014419185OMIM:219000Fraser syndrome.353
HP:0000183HP:0000183Difficulty in tongue movements0GAA CL E G H25484065ORPHA:308552Glycogen storage disease due to acid maltase deficiency, infantile onsetHP:0040282 - Frequent407
HP:0000183HP:0000183Difficulty in tongue movements0GIPC1 CL E G H107551226ORPHA:98897Oculopharyngodistal myopathyHP:0040282 - Frequent
HP:0000183HP:0000183Difficulty in tongue movements0GNAI3 CL E G H27734387ORPHA:137888Auriculocondylar syndromeHP:0040282 - Frequent2
HP:0000183HP:0000183Difficulty in tongue movements0NOTCH2NLC CL E G H10099671753924ORPHA:98897Oculopharyngodistal myopathyHP:0040282 - Frequent
HP:0000183HP:0000183Difficulty in tongue movements0PLCB4 CL E G H53329059ORPHA:137888Auriculocondylar syndromeHP:0040282 - Frequent82
HP:0000183HP:0000183Difficulty in tongue movements0SBF2 CL E G H818462135ORPHA:99956Charcot-Marie-Tooth disease type 4B2180
HP:0000183HP:0000183Difficulty in tongue movements0SH3TC2 CL E G H7962829427ORPHA:99949Charcot-Marie-Tooth disease type 4CHP:0040283 - Occasional493


Genes (11) :ALS2 ATP13A2 EDN1 FRAS1 GAA GIPC1 GNAI3 NOTCH2NLC PLCB4 SBF2 SH3TC2

Diseases (9) :OMIM:205100 OMIM:606353 ORPHA:306674 ORPHA:137888 OMIM:219000 ORPHA:308552 ORPHA:98897 ORPHA:99956 ORPHA:99949
 

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