Sleep apnea

Symptom Information:

Symptom ID: HPO:0010535
Synonyms:
Sleep apnoea [HPO:0010535]
Sleep apnea (disorder) [Orphanet:33200]
Sleep Apnea Syndromes [Orphanet:33200]
Sleep apnea [OMIM:Sleep apnea]
Apnea/sleep apnea [Orphanet:33200]
Sleep apnoea syndrome [Orphanet:33200]
Sleep apnoea syndrome [MedDRA:10040979]
Central sleep apnoea syndrome [MedDRA:10040979]
Hypersomnia with sleep apnea [MedDRA:10040979]
Insomnia with sleep apnea [MedDRA:10040979]
Obstructive sleep apnoea syndrome [MedDRA:10040979]
Other and unspecified sleep apnea [MedDRA:10040979]
Sleep apnea [MedDRA:10040979]
Sleep apnea syndrome [MedDRA:10040979]
Sleep apnoea [MedDRA:10040979]
Sleep apnoea syndromes [MedDRA:10040979]
Apnoea syndrome [MedDRA:10040979]
Apnea syndrome [MedDRA:10040979]
Central sleep apnea syndrome [MedDRA:10040979]
Obstructive sleep apnea syndrome [MedDRA:10040979]
Hypopnea syndrome [MedDRA:10040979]
Hypopnoea syndrome [MedDRA:10040979]
Sleep apnea (in 1/4 patients) [OMIM:Sleep apnea (in 1/4 patients)]
Sleep apnea (rare) [OMIM:Sleep apnea (rare)]
Sleep apnoeas [MedDRA:10040978]
Quality:
Cross references:
HPO:0010536 "Central sleep apnea" [Orphanet:33200]
Orphanet:33200 "Apnea/sleep apnea" [Orphanet:33200]
OMIM: "Sleep apnea" [OMIM:Sleep apnea]
OMIM: "Sleep apnea (in 1/4 patients)" [OMIM:Sleep apnea (in 1/4 patients)]
OMIM: "Sleep apnea (rare)" [OMIM:Sleep apnea (rare)]
UMLS:C0037315 "Sleep Apnea Syndromes" [Orphanet:33200]
Is a (Direct Parents):
MedDRA Sleep disturbance
Orphanet Apnea
HPO         Apnea
Orphanet Abnormality of the respiratory system
HPO         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)
                      Sleep apnea(HPO:0010535)
       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)
MedDRA:
Nervous system disorders(MedDRA:10029205)
    Sleep disturbance(HPO:0002360)
       Sleep apnea(HPO:0010535)
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)