Human Phenotype Ontology 
Grandparent Node:
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Behavioral abnormality (HP:0000708)help
Parent Node:
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Delusions (HP:0000746)help
..Starting node
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Paranoia (HP:0011999)help
Term ID: 11999
Name: Paranoia
Synonym: Paranoia
Definition: A persecutory delusion of supposed hostility of others.
Comments:
Reference: HP:0011999
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:0011999HP:0011999Paranoia0ATRX CL E G H546886ORPHA:96253Cushing disease169
HP:0011999HP:0011999Paranoia0BRAF CL E G H6731097ORPHA:96253Cushing disease276
HP:0011999HP:0011999Paranoia0CDH23 CL E G H6407213733ORPHA:96253Cushing disease636
HP:0011999HP:0011999Paranoia0CPOX CL E G H13712321OMIM:121300Coproporphyria.72
HP:0011999HP:0011999Paranoia0DGCR2 CL E G H99932845OMIM:192430Velocardiofacial syndrome.
HP:0011999HP:0011999Paranoia0DGCR6 CL E G H82142846OMIM:192430Velocardiofacial syndrome.
HP:0011999HP:0011999Paranoia0DGCR8 CL E G H544872847OMIM:192430Velocardiofacial syndrome.
HP:0011999HP:0011999Paranoia0ECM1 CL E G H18933153OMIM:247100Urbach-Wiethe disease.14
HP:0011999HP:0011999Paranoia0ESS2 CL E G H822016817OMIM:192430Velocardiofacial syndrome.
HP:0011999HP:0011999Paranoia0FMO3 CL E G H23283771ORPHA:468726Severe primary trimethylaminuriaHP:0040283 - Occasional55
HP:0011999HP:0011999Paranoia0HMBS CL E G H31454982ORPHA:79276Acute intermittent porphyriaHP:0040283 - Occasional81
HP:0011999HP:0011999Paranoia0IMPA1 CL E G H36126050OMIM:617323Mental retardation, autosomal recessive 59.1
HP:0011999HP:0011999Paranoia0NR3C1 CL E G H29087978ORPHA:96253Cushing disease79
HP:0011999HP:0011999Paranoia0PLA2G6 CL E G H83989039ORPHA:199351Adult-onset dystonia-parkinsonismHP:0040283 - Occasional133
HP:0011999HP:0011999Paranoia0PPOX CL E G H54989280ORPHA:79473Porphyria variegataHP:0040284 - Very rare41
HP:0011999HP:0011999Paranoia0PRDM8 CL E G H5697813993ORPHA:324290Early-onset Lafora body diseaseHP:0040284 - Very rare1
HP:0011999HP:0011999Paranoia0PRDM8 CL E G H5697813993OMIM:616640Epilepsy, progressive myoclonic, 101
HP:0011999HP:0011999Paranoia0SNCA CL E G H662211138OMIM:605543Parkinson disease 4.65
HP:0011999HP:0011999Paranoia0TBP CL E G H690811588OMIM:607136Spinocerebellar ataxia 17.7
HP:0011999HP:0011999Paranoia0TBX1 CL E G H689911592OMIM:192430Velocardiofacial syndrome.32
HP:0011999HP:0011999Paranoia0TIMM8A CL E G H167811817ORPHA:52368Mohr-Tranebjaerg syndromeHP:0040283 - Occasional15
HP:0011999HP:0011999Paranoia0TP53 CL E G H715711998ORPHA:96253Cushing disease911
HP:0011999HP:0011999Paranoia0USP48 CL E G H8419618533ORPHA:96253Cushing disease1
HP:0011999HP:0011999Paranoia0USP8 CL E G H910112631ORPHA:96253Cushing disease7
HP:0011999HP:0011999Paranoia0VPS13A CL E G H232301908ORPHA:2388ChoreoacanthocytosisHP:0040283 - Occasional130


Genes (24) :ATRX BRAF CDH23 CPOX DGCR2 DGCR6 DGCR8 ECM1 ESS2 FMO3 HMBS IMPA1 NR3C1 PLA2G6 PPOX PRDM8 SNCA TBP TBX1 TIMM8A TP53 USP48 USP8 VPS13A

Diseases (15) :ORPHA:96253 OMIM:121300 OMIM:192430 OMIM:247100 ORPHA:468726 ORPHA:79276 OMIM:617323 ORPHA:199351 ORPHA:79473 ORPHA:324290 OMIM:616640 OMIM:605543 OMIM:607136 ORPHA:52368 ORPHA:2388
 

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