Human Phenotype Ontology 
Grandparent Node:
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Cerebral atrophy (HP:0002059)help
Parent Node:
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Cerebral cortical atrophy (HP:0002120)help
..Starting node
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Temporal cortical atrophy (HP:0007112)help
Term ID: 7112
Name: Temporal cortical atrophy
Synonym:
Definition: Atrophy of the temporal cortex.
Comments:
Reference: HP:0007112
Genes and Diseases:
 
       Child Nodes:

 Sister Nodes: 
..expandCerebral cortical hemiatrophy (HP:0100308) help
..expandFrontal cortical atrophy (HP:0006913) help
..expandOccipital cortical atrophy (HP:0012105) help
..expandParietal cortical atrophy (HP:0012104) 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:0007112HP:0007112Temporal cortical atrophy0ABCA7 CL E G H1034737OMIM:608907Alzheimer disease 9, susceptibility to3
HP:0007112HP:0007112Temporal cortical atrophy0ADARB1 CL E G H104226OMIM:618862NEURODEVELOPMENTAL DISORDER WITH HYPOTONIA, MICROCEPHALY, AND SEIZURES; NEDHYMS1
HP:0007112HP:0007112Temporal cortical atrophy0BICRA CL E G H299984332OMIM:619325COFFIN-SIRIS SYNDROME 12; CSS122
HP:0007112HP:0007112Temporal cortical atrophy0C9ORF72 CL E G H20322828337ORPHA:100070Progressive non-fluent aphasiaHP:0040281 - Very frequent56
HP:0007112HP:0007112Temporal cortical atrophy0CAMTA1 CL E G H2326118806OMIM:614756Cerebellar ataxia, nonprogressive, with mental retardation34
HP:0007112HP:0007112Temporal cortical atrophy0CHMP2B CL E G H2597824537ORPHA:100070Progressive non-fluent aphasiaHP:0040281 - Very frequent42
HP:0007112HP:0007112Temporal cortical atrophy0COG1 CL E G H93826545ORPHA:263508COG1-CDGHP:0040283 - Occasional52
HP:0007112HP:0007112Temporal cortical atrophy0CPA6 CL E G H5709417245OMIM:614418FEBRILE SEIZURES, FAMILIAL, 11; FEB1149
HP:0007112HP:0007112Temporal cortical atrophy0CYB5A CL E G H15282570ORPHA:621Hereditary methemoglobinemiaHP:0040283 - Occasional2
HP:0007112HP:0007112Temporal cortical atrophy0CYB5R3 CL E G H17272873ORPHA:621Hereditary methemoglobinemiaHP:0040283 - Occasional24
HP:0007112HP:0007112Temporal cortical atrophy0GRM7 CL E G H29174599OMIM:618922NEURODEVELOPMENTAL DISORDER WITH SEIZURES, HYPOTONIA, AND BRAIN IMAGING ABNORMALITIES; NEDSHBA5
HP:0007112HP:0007112Temporal cortical atrophy0GRN CL E G H28964601ORPHA:100070Progressive non-fluent aphasiaHP:0040281 - Very frequent126
HP:0007112HP:0007112Temporal cortical atrophy0MAPT CL E G H41376893ORPHA:100070Progressive non-fluent aphasiaHP:0040281 - Very frequent140
HP:0007112HP:0007112Temporal cortical atrophy0NEK1 CL E G H47507744OMIM:617892Amyotrophic lateral sclerosis, susceptibility to, 24101
HP:0007112HP:0007112Temporal cortical atrophy0OPHN1 CL E G H49838148ORPHA:137831X-linked intellectual disability-cerebellar hypoplasia syndromeHP:0040283 - Occasional55
HP:0007112HP:0007112Temporal cortical atrophy0PDE6D CL E G H51478788OMIM:615665Joubert syndrome 221
HP:0007112HP:0007112Temporal cortical atrophy0PSEN1 CL E G H56639508ORPHA:100070Progressive non-fluent aphasiaHP:0040281 - Very frequent241
HP:0007112HP:0007112Temporal cortical atrophy0RNU4ATAC CL E G H10015168334016ORPHA:353298Roifman syndrome15
HP:0007112HP:0007112Temporal cortical atrophy0TMEM106B CL E G H5466422407ORPHA:100070Progressive non-fluent aphasiaHP:0040281 - Very frequent
HP:0007112HP:0007112Temporal cortical atrophy0TREM2 CL E G H5420917761ORPHA:100070Progressive non-fluent aphasiaHP:0040281 - Very frequent31
HP:0007112HP:0007112Temporal cortical atrophy0VCP CL E G H741512666OMIM:167320Inclusion body myopathy with early-onset paget disease with or without frontotemporal dementia 1.63
HP:0007112HP:0007112Temporal cortical atrophy0VCP CL E G H741512666ORPHA:100070Progressive non-fluent aphasiaHP:0040281 - Very frequent63
HP:0007112HP:0410170Hippocampal atrophy1ABCA7 CL E G H1034737OMIM:608907Alzheimer disease 9, susceptibility to.3
HP:0007112HP:0410170Hippocampal atrophy1BICRA CL E G H299984332OMIM:619325COFFIN-SIRIS SYNDROME 12; CSS122
HP:0007112HP:0410170Hippocampal atrophy1CAMTA1 CL E G H2326118806OMIM:614756Cerebellar ataxia, nonprogressive, with mental retardation.34
HP:0007112HP:0410170Hippocampal atrophy1CPA6 CL E G H5709417245OMIM:614418FEBRILE SEIZURES, FAMILIAL, 11; FEB1149
HP:0007112HP:0410170Hippocampal atrophy1GRM7 CL E G H29174599OMIM:618922NEURODEVELOPMENTAL DISORDER WITH SEIZURES, HYPOTONIA, AND BRAIN IMAGING ABNORMALITIES; NEDSHBA5
HP:0007112HP:0410170Hippocampal atrophy1NEK1 CL E G H47507744OMIM:617892Amyotrophic lateral sclerosis, susceptibility to, 24.101
HP:0007112HP:0410170Hippocampal atrophy1RNU4ATAC CL E G H10015168334016ORPHA:353298Roifman syndromeHP:0040282 - Frequent15


Genes (21) :ABCA7 ADARB1 BICRA C9ORF72 CAMTA1 CHMP2B COG1 CPA6 CYB5A CYB5R3 GRM7 GRN MAPT NEK1 OPHN1 PDE6D PSEN1 RNU4ATAC TMEM106B TREM2 VCP

Diseases (14) :OMIM:608907 OMIM:618862 OMIM:619325 ORPHA:100070 OMIM:614756 ORPHA:263508 OMIM:614418 ORPHA:621 OMIM:618922 OMIM:617892 ORPHA:137831 OMIM:615665 ORPHA:353298 OMIM:167320
 

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