Insomnia

Symptom Information:

Symptom ID: HPO:0100785
Synonyms:
Insomnia (disorder) [Orphanet:43460]
Sleeplessness [Orphanet:43460]
Insomnia [OMIM:Insomnia]
Insomnia [Orphanet:43460]
Insomnia [MedDRA:10022437]
Difficulty sleeping [MedDRA:10022437]
Insomnia (non-organic) [MedDRA:10022437]
Insomnia exacerbated [MedDRA:10022437]
Insomnia NEC [MedDRA:10022437]
Insomnia NOS [MedDRA:10022437]
Other insomnia [MedDRA:10022437]
Persistent disorder of initiating or maintaining sleep [MedDRA:10022437]
Primary insomnia [MedDRA:10022437]
Sleep decreased [MedDRA:10022437]
Sleep difficult [MedDRA:10022437]
Sleep loss [MedDRA:10022437]
Sleeplessness [MedDRA:10022437]
Transient disorder of initiating or maintaining sleep [MedDRA:10022437]
Chronic insomnia [MedDRA:10022437]
Dysphylaxia [MedDRA:10022437]
Transient insomnia [MedDRA:10022437]
Insomnia (HCP) [OMIM:Insomnia (HCP)]
Sleep difficulties [OMIM:Sleep difficulties]
Sleeping difficulties [OMIM:Sleeping difficulties]
Quality:
Cross references:
Orphanet:43460 "Insomnia" [Orphanet:43460]
OMIM: "Insomnia" [OMIM:Insomnia]
OMIM: "Insomnia (HCP)" [OMIM:Insomnia (HCP)]
OMIM: "Sleep difficulties" [OMIM:Sleep difficulties]
OMIM: "Sleeping difficulties" [OMIM:Sleeping difficulties]
UMLS:C0917801 "Sleeplessness" [Orphanet:43460]
Is a (Direct Parents):
MedDRA Disturbances in initiating and maintaining sleep
HPO         Sleep disturbance
Orphanet Sleep disturbance
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)
                   Sleep disturbance(HPO:0002360)
                      Insomnia(HPO:0100785)
MedDRA:
Nervous system disorders(MedDRA:10029205)
    Sleep disturbance(HPO:0002360)
       Disturbances in initiating and maintaining sleep(MedDRA:10013510)
          Insomnia(HPO:0100785)
Database Frequency: 18 / 7739
Resource:

All diseases associated with this symptom:

15q24 microdeletion syndrome (Orphanet:94065)
Acute intermittent porphyria (Orphanet:79276)
Buerger disease (Orphanet:36258)
CK syndrome (Orphanet:251383)
EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 2 (OMIM:300672)
Familial hyperthyroidism due to mutations in TSH receptor (Orphanet:424)
Fatal familial insomnia (Orphanet:466)
Hereditary coproporphyria (Orphanet:79273)
Hypernychthemeral syndrome (Orphanet:73267)
Lyme disease (Orphanet:91546)
McLeod neuroacanthocytosis syndrome (Orphanet:59306)
Mucopolysaccharidosis type 2, severe form (Orphanet:217085)
Perry syndrome (Orphanet:178509)
RESTLESS LEGS SYNDROME, SUSCEPTIBILITY TO, 1 (OMIM:102300)
Rabies (Orphanet:770)
Typhoid (Orphanet:99745)
Williams syndrome (Orphanet:904)
Wolfram syndrome 1 (OMIM:222300)