Central apnea
Symptom Information:
Symptom ID: | HPO:0002871 | |||
Synonyms: |
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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 respiratory system(HPO:0002086) Functional respiratory abnormality(HPO:0002795) Abnormal pattern of respiration(HPO:0002793) Apnea(HPO:0002104) Central apnea(HPO:0002871) MedDRA: |
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Database Frequency: | 10 / 7739 | |||
Resource: |
All diseases associated with this symptom:
AURICULOCONDYLAR SYNDROME 2 | (OMIM:614669) |
Autosomal recessive spastic paraplegia type 49 | (Orphanet:320385) |
Joubert syndrome | (Orphanet:475) |
Joubert syndrome 1 | (OMIM:213300) |
Joubert syndrome 2 | (OMIM:608091) |
Joubert syndrome 3 | (OMIM:608629) |
Joubert syndrome 5 | (OMIM:610188) |
Joubert syndrome with ocular defect | (Orphanet:220493) |
KRABBE DISEASE, ATYPICAL, DUE TO SAPOSIN A DEFICIENCY | (OMIM:611722) |
Wolfram syndrome 1 | (OMIM:222300) |