Human Phenotype Ontology 
Grandparent Node:
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Abnormal muscle physiology (HP:0011804)help
Parent Node:
expand
Abnormal central motor function (HP:0011442)help
Parent Node:
expand
Abnormal muscle tone (HP:0003808)help
..Starting node
..expand
obsolete Central hypotonia (HP:0011398)help
Term ID: 11398
Name: obsolete Central hypotonia
Synonym:
Definition:
Comments:
Reference: HP:0011398
Genes and Diseases:
 
       Child Nodes:

 Sister Nodes: 
..expandHypertonia (HP:0001276) help
..expandHypotonia (HP:0001252) 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:0011398HP:0011398obsolete Central hypotonia0 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.