Human Phenotype Ontology 
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..expandLong term memory impairment (HP:0033688)help
Term ID: 33688
Name: Long term memory impairment
Synonym: Long term memory loss
Definition: A deficit in the ability to retrieve information from long-term memory, which can be defined as a seemingly unlimited capacity to store memories can last years and relate to the performance of actions or skills (i.e., procedural memories, knowing how) and memories of facts, rules, concepts, and events (i.e., declarative memories, knowing that).
Comments:
Reference: HP:0033688
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:0033688HP:0033688Long term memory impairment0 CL E G H
HP:0033688HP:0033690Retrograde memory impairment1 CL E G H
HP:0033688HP:0033689Anterograde memory impairment1 CL E G H
HP:0033688HP:0033692Declarative memory loss2 CL E G H
HP:0033688HP:0033691Procedural memory loss2 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.