Human Phenotype Ontology 
Grandparent Node:
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Constitutional symptom (HP:0025142)help
Parent Node:
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Impairment of activities of daily living (HP:0031058)help
..Starting node
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Impaired transferring ability (HP:0031062)help
Term ID: 31062
Name: Impaired transferring ability
Synonym:
Definition: Applies to an individual who needs help in moving from bed to chair or requires a complete transfer.
Comments:
Reference: HP:0031062
Genes and Diseases:
 
       Child Nodes:

 Sister Nodes: 
..expandImpaired ability to bathe oneself (HP:0031059) help
..expandImpaired ability to dress oneself (HP:0031060) help
..expandImpaired continence (HP:0031064) help
..expandImpaired feeding ability (HP:0031063) help
..expandImpaired toileting ability (HP:0031061) 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:0031062HP:0031062Impaired transferring ability0 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.