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
..expandAxial hypotonia (HP:0008936) help
..expandFacial hypotonia (HP:0000297) help
..expandFrog-leg posture (HP:0031139) help
..expandGeneralized hypotonia (HP:0001290) help
..expandInfantile muscular hypotonia (HP:0008947) help
..expandNeonatal hypotonia (HP:0001319) help
..expandSevere muscular hypotonia (HP:0006829) 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:0030190HP:0030190Oral motor hypotonia0BICRA CL E G H299984332OMIM:619325COFFIN-SIRIS SYNDROME 12; CSS122
HP:0030190HP:0030190Oral motor hypotonia0CTNS CL E G H14972518OMIM:219800Cystinosis, nephropathic178
HP:0030190HP:0030190Oral motor hypotonia0HTT CL E G H30644851ORPHA:248111Juvenile Huntington diseaseHP:0040282 - Frequent12


Genes (3) :BICRA CTNS HTT

Diseases (3) :OMIM:619325 OMIM:219800 ORPHA:248111
 

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