Human Phenotype Ontology 
Grandparent Node:
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Behavioral abnormality (HP:0000708)help
Parent Node:
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Abnormal emotion/affect behavior (HP:0100851)help
..Starting node
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Mood swings (HP:0000720)help
Term ID: 720
Name: Mood swings
Synonym: Mood swings
Definition: An exaggeration of emotional affects such as laughing crying, or yawning beyond what the person feels.
Comments:
Reference: HP:0000720
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
..expandMood changes (HP:0001575) help
..expandSuicidal ideation (HP:0031589) help
..expandUnhappy demeanor (HP:0031588) help
InputHPO IDHPO termDistanceGeneGene id entrezDiseaseIdDiseaseNameDiseaseMIMConceptIDSourceTypical associationHGMD variantsClinVar variantsHGNC IDGeneMIM
 
HPO disease - gene - phenotype typical associations:
HP:0000720HP:0000720Mood swings0CUL4B CL E G H8450300354Syndromic X-linked mental retardation, Cabezas type300354C1845861OMIM1402472555300304
HP:0000720HP:0000720Mood swings0DEAF1 CL E G H10522617171Dyskinesia, seizures, and intellectual developmental disorder617171C4310683OMIM11712914677602635
HP:0000720HP:0000720Mood swings0DEAF1 CL E G H10522615828Mental retardation, autosomal dominant 24615828C4014414OMIM11712914677602635
HP:0000720HP:0000720Mood swings0DGCR2 CL E G H9993192430Shprintzen syndrome192430C0220704OMIM133902845600594
HP:0000720HP:0000720Mood swings0DGCR6 CL E G H8214192430Shprintzen syndrome192430C0220704OMIM133172846601279
HP:0000720HP:0000720Mood swings0DGCR8 CL E G H54487192430Shprintzen syndrome192430C0220704OMIM123812847609030
HP:0000720HP:0000720Mood swings0ESS2 CL E G H8220192430Shprintzen syndrome192430C0220704OMIM1138216817601755
HP:0000720HP:0000720Mood swings0TBX1 CL E G H6899192430Shprintzen syndrome192430C0220704OMIM18255311592602054
HP:0000720HP:0000720Mood swings0ZFYVE26 CL E G H23503270700Spastic paraplegia 15270700C1849128OMIM14570020761612012
 
HPO disease - gene - phenotype less frequent non-typical associations:
HP:0000720HP:0000720Mood swings0BPTF CL E G H2186529962ORPHA014803581601819
HP:0000720HP:0000720Mood swings0PSMD12 CL E G H5718529962ORPHA010359557604450


Genes (10) :BPTF CUL4B DEAF1 DGCR2 DGCR6 DGCR8 ESS2 PSMD12 TBX1 ZFYVE26

Diseases (6) :529962 300354 617171 615828 192430 270700
 

Human Phenotype Ontology(HPO) is developed by the Human Phenotype Ontology Consortium. The version used here is June 2019 release.