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
..expand
Happy demeanor (HP:0040082)help
Term ID: 40082
Name: Happy demeanor
Synonym: Happy demeanor
Definition: A conspicuously happy disposition with frequent smiling and laughing that may be context-inappropriate or unrelated to context.
Comments:
Reference: HP:0040082
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
..expandIrritability (HP:0000737) help
..expandMood changes (HP:0001575) help
..expandMood swings (HP:0000720) 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:0040082HP:0040082Happy demeanor0HDAC8 CL E G H55869300882Cornelia de Lange syndrome 5300882C3550903OMIM15622713315300269
HP:0040082HP:0040082Happy demeanor0RAB11B CL E G H9230617807NEURODEVELOPMENTAL DISORDER WITH ATAXIC GAIT, ABSENT SPEECH, AND DECREASED CORTICAL WHITE MATTER617807C4540498OMIM12149761604198
HP:0040082HP:0040082Happy demeanor0SATB2 CL E G H23314612313Chromosome 2q32-q33 deletion syndrome612313C2676739OMIM110627421637608148
HP:0040082HP:0040082Happy demeanor0SLC9A6 CL E G H10479300243Christianson syndrome300243C2678194OMIM12835111079300231
HP:0040082HP:0040082Happy demeanor0TBC1D23 CL E G H55773617695PONTOCEREBELLAR HYPOPLASIA, TYPE 11617695C4540164OMIM192525622617687
HP:0040082HP:0040082Happy demeanor0WDR26 CL E G H80232617616SKRABAN-DEARDORFF SYNDROME617616C4539927OMIM1346921208617424
HP:0040082HP:0040082Happy demeanor0ZEB2 CL E G H9839235730Mowat-Wilson syndrome235730C1856113OMIM129861314881605802
HP:0040082HP:0040082Happy demeanor0ZSWIM6 CL E G H57688617865NEURODEVELOPMENTAL DISORDER WITH MOVEMENT ABNORMALITIES, ABNORMAL GAIT, AND AUTISTIC FEATURES617865CN800196OMIM126229316615951
 
HPO disease - gene - phenotype less frequent non-typical associations:
HP:0040082HP:0040082Happy demeanor0ADSL CL E G H158103050Adenylosuccinate lyase deficiency103050C0268126OMIM058279291608222
HP:0040082HP:0040082Happy demeanor0DYRK1A CL E G H1859614104Mental retardation, autosomal dominant 7614104C3279839OMIM0774373091600855
HP:0040082HP:0040082Happy demeanor0TCF4 CL E G H69252896Hypogonadism retinitis pigmentosaORPHA014862411634602272


Genes (11) :ADSL DYRK1A HDAC8 RAB11B SATB2 SLC9A6 TBC1D23 TCF4 WDR26 ZEB2 ZSWIM6

Diseases (11) :103050 614104 300882 617807 612313 300243 617695 2896 617616 235730 617865
 

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