Sleep apnea
Symptom Information:
Symptom ID: | HPO:0010535 | |||||||||||||||||||||||||
Synonyms: |
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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 respiratory system(HPO:0002086) Functional respiratory abnormality(HPO:0002795) Abnormal pattern of respiration(HPO:0002793) Apnea(HPO:0002104) Sleep apnea(HPO:0010535) 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) Sleep apnea(HPO:0010535) MedDRA: Nervous system disorders(MedDRA:10029205) Sleep disturbance(HPO:0002360) Sleep apnea(HPO:0010535) |
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Database Frequency: | 24 / 7739 | |||||||||||||||||||||||||
Resource: |
All diseases associated with this symptom:
17p11.2 microduplication syndrome | (Orphanet:1713) |
48,XXYY syndrome | (Orphanet:10) |
AMYOTROPHIC LATERAL SCLEROSIS 1 | (OMIM:105400) |
APNEA, CENTRAL SLEEP | (OMIM:107640) |
APNEA, CENTRAL SLEEP | (OMIM:207720) |
Amyotrophic lateral sclerosis | (Orphanet:803) |
BARATELA-SCOTT SYNDROME | (OMIM:300881) |
Bardet-Biedl syndrome 10 | (OMIM:615987) |
Bardet-Biedl syndrome 2 | (OMIM:615981) |
Bardet-Biedl syndrome 4 | (OMIM:615982) |
Bardet-Biedl syndrome 5 | (OMIM:615983) |
Cardiofaciocutaneous syndrome | (Orphanet:1340) |
Crouzon disease | (Orphanet:207) |
Dysmorphism - conductive hearing loss - heart defect | (Orphanet:289553) |
Glaucoma - sleep apnea | (Orphanet:2085) |
Idiopathic pulmonary fibrosis | (Orphanet:2032) |
Joubert syndrome 28 | (OMIM:617121) |
MELAS | (Orphanet:550) |
MOSAIC VARIEGATED ANEUPLOIDY SYNDROME 2 | (OMIM:614114) |
McLeod neuroacanthocytosis syndrome | (Orphanet:59306) |
Mucopolysaccharidosis type 2 | (Orphanet:580) |
Prader-Willi syndrome | (Orphanet:739) |
SCHAAF-YANG SYNDROME | (OMIM:615547) |
Sialuria | (Orphanet:3166) |