Human Phenotype Ontology 
Grandparent Node:
expandAbnormal muscle tone (HP:0003808)help
Parent Node:
expandHypotonia (HP:0001252)help
..Starting node
..expandOral motor hypotonia (HP:0030190)help
Term ID: 30190
Name: Oral motor hypotonia
Synonym:
Definition: Reduced muscle tone of oral musculature. In infants, this feature may be associated with difficulties in breast feeding, and may affect the latch, jaw motions, tongue placement, lip seal, suck/swallow/breathe pattern and overall feeding behavior.
Comments:
Reference: HP:0030190
Genes and Diseases:
 
       Child Nodes:

 Sister Nodes: 
..expandAppendicular hypotonia (HP:0012389) help
..expandFacial hypotonia (HP:0000297) help
..expandFrog-leg posture (HP:0031139) help
..expandGeneralized hypotonia (HP:0001290) help
..expandInfantile muscular hypotonia (HP:0008947) help
..expandMuscular hypotonia of the trunk (HP:0008936) help
..expandNeonatal hypotonia (HP:0001319) help
..expandSevere muscular hypotonia (HP:0006829) help
InputHPO IDHPO termDistanceGeneGene id entrezDiseaseIdDiseaseNameDiseaseMIMConceptIDSourceTypical associationHGMD variantsClinVar variantsHGNC IDGeneMIM
 
HPO disease - gene - phenotype typical associations:
HP:0030190HP:0030190Oral motor hypotonia0CTNS CL E G H1497219800Nephropathic cystinosis219800C0010690OMIM17782518606272
HP:0030190HP:0030190Oral motor hypotonia0HTT CL E G H3064248111ORPHA17604851613004
 
HPO disease - gene - phenotype less frequent non-typical associations:


Genes (2) :CTNS HTT

Diseases (2) :219800 248111
 

Human Phenotype Ontology(HPO) is developed by the Human Phenotype Ontology Consortium. The version used here is August 2021 release.