Nocturnal hypoventilation
Symptom Information:
Symptom ID: | HPO:0002877 | ||
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 respiratory system(HPO:0002086) Functional respiratory abnormality(HPO:0002795) Abnormal pattern of respiration(HPO:0002793) Hypoventilation(HPO:0002791) Nocturnal hypoventilation(HPO:0002877) MedDRA: |
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Database Frequency: | 9 / 7739 | ||
Resource: |
All diseases associated with this symptom:
Autosomal recessive limb-girdle muscular dystrophy type 2I | (Orphanet:34515) |
BROWN-VIALETTO-VAN LAERE SYNDROME 1 | (OMIM:211530) |
Classic multiminicore myopathy | (Orphanet:324604) |
Congenital muscular dystrophy, Ullrich type | (Orphanet:75840) |
Desmin-related myopathy with Mallory body-like inclusions | (Orphanet:84132) |
Distal myopathy with early respiratory muscle involvement | (Orphanet:34521) |
Duchenne muscular dystrophy | (Orphanet:98896) |
Riboflavin transporter deficiency | (Orphanet:97229) |
Rigid spine syndrome | (Orphanet:97244) |