Anxiety

Symptom Information:

Symptom ID: HPO:0000739
Synonyms:
Anxiety disease [HPO:0000739]
Anxiety disorder [Orphanet:43620]
Anxiety disorder (disorder) [Orphanet:43620]
anxiety [HPO:0000739]
Anxiety symptoms [Orphanet:43620]
Anxiety Disorders [Orphanet:43620]
Anxiety [OMIM:Anxiety]
Humour troubles/anxiety/depression/apathy/euphoria/irritability [Orphanet:43620]
Anxiety symptoms NOS [Orphanet:43620]
Anxiety [MedDRA:10002855]
Alarm (not alarm reaction) [MedDRA:10002855]
Angor animi [MedDRA:10002855]
Anguish [MedDRA:10002855]
Anxiety attack [MedDRA:10002855]
Anxiety complex [MedDRA:10002855]
Anxiety NEC [MedDRA:10002855]
Anxiety reaction [MedDRA:10002855]
Anxiety state [MedDRA:10002855]
Anxiety state, unspecified [MedDRA:10002855]
Anxiety states [MedDRA:10002855]
Anxiety symptoms NOS [MedDRA:10002855]
Anxiety-ridden [MedDRA:10002855]
Anxious mood [MedDRA:10002855]
Apprehension [MedDRA:10002855]
Exacerbation of anxiety [MedDRA:10002855]
Face anguish [MedDRA:10002855]
Feeling anxious [MedDRA:10002855]
Feeling of intense apprehension [MedDRA:10002855]
Impending doom [MedDRA:10002855]
Made anxiety worse [MedDRA:10002855]
Other anxiety states [MedDRA:10002855]
Phobic anxiety [MedDRA:10002855]
Reaction alarm [MedDRA:10002855]
Reaction anxiety [MedDRA:10002855]
Separation anxiety [MedDRA:10002855]
Situational anxiety [MedDRA:10002855]
Worry [MedDRA:10002855]
Anxiety aggravated [MedDRA:10002855]
Chronic anxiety [MedDRA:10002855]
Anxiety disorder [MedDRA:10057666]
Anxiety disorder NEC [MedDRA:10057666]
Anxiety neurosis [MedDRA:10057666]
Anxious personality [MedDRA:10057666]
Introspective &
anxiety-prone patient [MedDRA:10057666]
Anxiety disorder aggravated [MedDRA:10057666]
Anxiety (64%) [OMIM:Anxiety (64%)]
Anxiety (HCP) [OMIM:Anxiety (HCP)]
Anxiety (in some patients) [OMIM:Anxiety (in some patients)]
Anxiety attacks [OMIM:Anxiety attacks]
Anxiety disorders [OMIM:Anxiety disorders]
Euphoria [Orphanet:43620]
Euphoria [OMIM:Euphoria]
Anxiety symptoms [MedDRA:10002869]
Anxiety disorders NEC [MedDRA:10068761]
Quality:
Cross references:
Orphanet:43620 "Humour troubles/anxiety/depression/apathy/euphoria/irritability" [Orphanet:43620]
OMIM: "Anxiety" [OMIM:Anxiety]
OMIM: "Anxiety (64%)" [OMIM:Anxiety (64%)]
OMIM: "Anxiety (HCP)" [OMIM:Anxiety (HCP)]
OMIM: "Anxiety (in some patients)" [OMIM:Anxiety (in some patients)]
OMIM: "Anxiety attacks" [OMIM:Anxiety attacks]
OMIM: "Anxiety disorders" [OMIM:Anxiety disorders]
OMIM: "Euphoria" [OMIM:Euphoria]
UMLS:C0860603 "anxiety" [HPO:0000739]
UMLS:C0860603 "Anxiety symptoms" [Orphanet:43620]
UMLS:C0003469 "Anxiety Disorders" [Orphanet:43620]
Is a (Direct Parents):
HPO         Abnormal fear/anxiety-related behavior
Orphanet Behavioral abnormality
Orphanet Depression
MedDRA Anxiety disorders and symptoms
Is a (Whole tree): HPO:
All(HPO:0000001)
    Phenotypic abnormality(HPO:0000118)
       Abnormality of the nervous system(HPO:0000707)
          Abnormality of nervous system physiology(HPO:0012638)
             Abnormality of higher mental function(HPO:0011446)
                Behavioral abnormality(HPO:0000708)
                   Abnormal emotion/affect behavior(HPO:0100851)
                      Abnormal fear/anxiety-related behavior(HPO:0100852)
                         Anxiety(HPO:0000739)
MedDRA:
Database Frequency: 67 / 7739
Resource:

All diseases associated with this symptom:

3q29 microdeletion syndrome (Orphanet:65286)
4-hydroxybutyric aciduria (Orphanet:22)
48,XXYY syndrome (Orphanet:10)
ACTH-independent macronodular adrenal hyperplasia (Orphanet:189427)
Aceruloplasminemia (Orphanet:48818)
Acute intermittent porphyria (Orphanet:79276)
Adiposis dolorosa (Orphanet:36397)
Alström syndrome (Orphanet:64)
BASAL GANGLIA CALCIFICATION, IDIOPATHIC, 5 (OMIM:615483)
Bardet-Biedl syndrome 1 (OMIM:209900 )
Bardet-Biedl syndrome 10 (OMIM:615987)
Bardet-Biedl syndrome 7 (OMIM:615984)
Benign familial chorea (Orphanet:1429)
CADASIL (Orphanet:136)
CELIAC DISEASE, SUSCEPTIBILITY TO, 1 (OMIM:212750)
CLN3 disease (Orphanet:228346)
Cerebro-facio-thoracic dysplasia (Orphanet:1394)
Choreoacanthocytosis (Orphanet:2388)
Classical phenylketonuria (Orphanet:79254)
Creutzfeldt-Jakob disease (Orphanet:204)
Cushing disease (Orphanet:96253)
Cushing syndrome (Orphanet:553)
Dopa-responsive dystonia due to sepiapterin reductase deficiency (Orphanet:70594)
Familial dyskinesia and facial myokymia (Orphanet:324588)
Familial or sporadic hemiplegic migraine (Orphanet:569)
Fragile X-associated tremor/ataxia syndrome (Orphanet:93256)
GLUCOCORTICOID RESISTANCE, GENERALIZED (OMIM:615962)
Growth delay due to insulin-like growth factor I resistance (Orphanet:73273)
Hereditary coproporphyria (Orphanet:79273)
Huntington disease (Orphanet:399)
Huntington disease-like 1 (Orphanet:157941)
Huntington disease-like 2 (Orphanet:98934)
Hyperammonemia due to N-acetylglutamate synthetase deficiency (Orphanet:927)
Infantile convulsions and choreoathetosis (Orphanet:31709)
Inherited Creutzfeldt-Jakob disease (Orphanet:282166)
LUBS X-LINKED MENTAL RETARDATION SYNDROME (OMIM:300260)
MELAS (Orphanet:550)
MENTAL RETARDATION, AUTOSOMAL RECESSIVE 41 (OMIM:615637)
MENTAL RETARDATION, X-LINKED 30 (OMIM:300558)
MIGRAINE, FAMILIAL HEMIPLEGIC, 1 (OMIM:141500)
MITOCHONDRIAL COMPLEX III DEFICIENCY, NUCLEAR TYPE 2 (OMIM:615157)
Maternal hyperphenylalaninemia (Orphanet:2209)
McLeod neuroacanthocytosis syndrome (Orphanet:59306)
Mohr-Tranebjaerg syndrome (Orphanet:52368)
Monosomy 5p (Orphanet:281)
Myoclonus-dystonia syndrome (Orphanet:36899)
Nasu-Hakola disease (Orphanet:2770)
PANIC DISORDER 1 (OMIM:167870)
PARKINSON DISEASE 6, AUTOSOMAL RECESSIVE EARLY-ONSET (OMIM:605909)
PARKINSON DISEASE 7, AUTOSOMAL RECESSIVE EARLY-ONSET (OMIM:606324)
PIGMENTED NODULAR ADRENOCORTICAL DISEASE, PRIMARY, 1 (OMIM:610489)
PIGMENTED NODULAR ADRENOCORTICAL DISEASE, PRIMARY, 2 (OMIM:610475)
PROGRESSIVE EXTERNAL OPHTHALMOPLEGIA WITH MITOCHONDRIAL DNA DELETIONS,AUTOSOMAL DOMINANT, 5 (OMIM:613077)
Phenylketonuria (Orphanet:716)
Primary pigmented nodular adrenocortical disease (Orphanet:189439)
Rapid-onset dystonia-parkinsonism (Orphanet:71517)
Recessive mitochondrial ataxia syndrome (Orphanet:94125)
Renpenning syndrome (Orphanet:3242)
SOTOS SYNDROME 2 (OMIM:614753)
Spinocerebellar ataxia type 12 (Orphanet:98762)
Stiff person syndrome (Orphanet:3198)
TENORIO SYNDROME (OMIM:616260)
TMCO1 defect syndrome (Orphanet:228407)
Williams syndrome (Orphanet:904)
Wolfram syndrome 1 (OMIM:222300)
Wolfram-like syndrome (ORPHA:411590)
[DEL] Wolfram-like syndrome, autosomal dominant (OMIM:614296)