Insomnia
Symptom Information:
Symptom ID: | HPO:0100785 | ||||||||||||||||||||||||
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) 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) |
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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) |