Human Phenotype Ontology 
Grandparent Node:
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Behavioral abnormality (HP:0000708)help
Parent Node:
expand
Abnormal emotion/affect behavior (HP:0100851)help
..Starting node
..expand
Suicidal ideation (HP:0031589)help
Term ID: 31589
Name: Suicidal ideation
Synonym: Suicidality
Definition: Frequent thinking about or preoccupation with killing oneself.
Comments:
Reference: HP:0031589
Genes and Diseases:
 
       Child Nodes:

 Sister Nodes: 
..expandAbnormal aggressive, impulsive or violent behavior (HP:0006919) help
..expandConspicuously happy disposition (HP:0100024) help
..expandDiminished motivation (HP:0000745) help
..expandEmotional blunting (HP:0030213) help
..expandEuphoria (HP:0031844) help
..expandHappy demeanor (HP:0040082) help
..expandIrritability (HP:0000737) help
..expandobsolete Mood changes (HP:0001575) help
..expandobsolete Mood swings (HP:0000720) help
..expandUnhappy demeanor (HP:0031588) 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:0031589HP:0031589Suicidal ideation0ATRX CL E G H546886ORPHA:96253Cushing disease169
HP:0031589HP:0031589Suicidal ideation0BRAF CL E G H6731097ORPHA:96253Cushing disease276
HP:0031589HP:0031589Suicidal ideation0CABP4 CL E G H570101386ORPHA:98784Autosomal dominant nocturnal frontal lobe epilepsyHP:0040283 - Occasional94
HP:0031589HP:0031589Suicidal ideation0CDH23 CL E G H6407213733ORPHA:96253Cushing disease636
HP:0031589HP:0031589Suicidal ideation0CEP85L CL E G H38711921638OMIM:618873LISSENCEPHALY 10; LIS101
HP:0031589HP:0031589Suicidal ideation0CHRNA2 CL E G H11351956ORPHA:98784Autosomal dominant nocturnal frontal lobe epilepsyHP:0040283 - Occasional188
HP:0031589HP:0031589Suicidal ideation0CHRNA4 CL E G H11371958ORPHA:98784Autosomal dominant nocturnal frontal lobe epilepsyHP:0040283 - Occasional225
HP:0031589HP:0031589Suicidal ideation0CHRNB2 CL E G H11411962ORPHA:98784Autosomal dominant nocturnal frontal lobe epilepsyHP:0040283 - Occasional88
HP:0031589HP:0031589Suicidal ideation0CRH CL E G H13922355ORPHA:98784Autosomal dominant nocturnal frontal lobe epilepsyHP:0040283 - Occasional1
HP:0031589HP:0031589Suicidal ideation0CYP27A1 CL E G H15932605ORPHA:909Cerebrotendinous xanthomatosisHP:0040283 - Occasional114
HP:0031589HP:0031589Suicidal ideation0DCDC2 CL E G H5147318141ORPHA:84081Senior-Boichis syndrome8
HP:0031589HP:0031589Suicidal ideation0DCTN1 CL E G H16392711OMIM:168605Perry syndrome86
HP:0031589HP:0031589Suicidal ideation0DEPDC5 CL E G H968118423ORPHA:98784Autosomal dominant nocturnal frontal lobe epilepsyHP:0040283 - Occasional172
HP:0031589HP:0031589Suicidal ideation0FIG4 CL E G H989616873ORPHA:208441Bilateral parasagittal parieto-occipital polymicrogyriaHP:0040283 - Occasional111
HP:0031589HP:0031589Suicidal ideation0HTT CL E G H30644851ORPHA:399Huntington diseaseHP:0040283 - Occasional12
HP:0031589HP:0031589Suicidal ideation0KCNT1 CL E G H5758218865ORPHA:98784Autosomal dominant nocturnal frontal lobe epilepsyHP:0040283 - Occasional321
HP:0031589HP:0031589Suicidal ideation0NR3C1 CL E G H29087978ORPHA:96253Cushing disease79
HP:0031589HP:0031589Suicidal ideation0SLC2A3 CL E G H651511007ORPHA:399Huntington diseaseHP:0040283 - Occasional1
HP:0031589HP:0031589Suicidal ideation0SPTBN1 CL E G H671111275OMIM:619475DEVELOPMENTAL DELAY, IMPAIRED SPEECH, AND BEHAVIORAL ABNORMALITIES; DDISBA
HP:0031589HP:0031589Suicidal ideation0TMEM67 CL E G H9114728396ORPHA:84081Senior-Boichis syndrome166
HP:0031589HP:0031589Suicidal ideation0TP53 CL E G H715711998ORPHA:96253Cushing disease911
HP:0031589HP:0031589Suicidal ideation0USP48 CL E G H8419618533ORPHA:96253Cushing disease1
HP:0031589HP:0031589Suicidal ideation0USP8 CL E G H910112631ORPHA:96253Cushing disease7


Genes (23) :ATRX BRAF CABP4 CDH23 CEP85L CHRNA2 CHRNA4 CHRNB2 CRH CYP27A1 DCDC2 DCTN1 DEPDC5 FIG4 HTT KCNT1 NR3C1 SLC2A3 SPTBN1 TMEM67 TP53 USP48 USP8

Diseases (9) :ORPHA:96253 ORPHA:98784 OMIM:618873 ORPHA:909 ORPHA:84081 OMIM:168605 ORPHA:208441 ORPHA:399 OMIM:619475
 

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