Human Phenotype Ontology 
Grandparent Node:
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Mental deterioration (HP:0001268)help
Parent Node:
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Dementia (HP:0000726)help
..Starting node
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Subcortical dementia (HP:0007123)help
Term ID: 7123
Name: Subcortical dementia
Synonym:
Definition: A particular type of dementia characterized by a pattern of mental defects consisting prominently of forgetfulness, slowness of thought processes, and personality or mood change.
Comments:
Reference: HP:0007123
Genes and Diseases:
 
       Child Nodes:

 Sister Nodes: 
..expandFrontal lobe dementia (HP:0000727) help
..expandFrontolimbic dementia (HP:0002439) help
..expandFrontotemporal dementia (HP:0002145) 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:0007123HP:0007123Subcortical dementia0FTL CL E G H25123999OMIM:606159Neurodegeneration with brain iron accumulation 3.33
HP:0007123HP:0007123Subcortical dementia0FTL CL E G H25123999ORPHA:157846NeuroferritinopathyHP:0040284 - Very rare33
HP:0007123HP:0007123Subcortical dementia0NOTCH3 CL E G H48547883OMIM:125310Cerebral arteriopathy, autosomal dominant, with subcortical infarctsand leukoencephalopathy.144


Genes (2) :FTL NOTCH3

Diseases (3) :OMIM:606159 ORPHA:157846 OMIM:125310
 

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