Anxiety
Symptom Information:
Symptom ID: | HPO:0000739 | |||||||||||||||||||||||||||||||||||||||||||||||||||||||
Synonyms: |
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Quality: | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Cross references: |
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Is a (Direct Parents): |
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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: |
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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) |