Diaphragmatic weakness
Symptom Information:
Symptom ID: | HPO:0009113 | |||||
Synonyms: |
|
|||||
Quality: | ||||||
Cross references: |
|
|||||
Is a (Direct Parents): |
|
|||||
Is a (Whole tree): |
HPO:
All(HPO:0000001) Phenotypic abnormality(HPO:0000118) Abnormality of the abdomen(HPO:0001438) Abnormality of the diaphragm(HPO:0000775) Diaphragmatic weakness(HPO:0009113) Abnormality of the musculature(HPO:0003011) Abnormality of muscle physiology(HPO:0011804) Muscle weakness(HPO:0001324) Diaphragmatic weakness(HPO:0009113) Abnormality of the respiratory system(HPO:0002086) Abnormal respiratory system morphology(HPO:0012252) Abnormality of the diaphragm(HPO:0000775) Diaphragmatic weakness(HPO:0009113) MedDRA: |
|||||
Database Frequency: | 12 / 7739 | |||||
Resource: |
All diseases associated with this symptom:
Autosomal dominant Charcot-Marie-Tooth disease type 2C | (Orphanet:99937) |
BROWN-VIALETTO-VAN LAERE SYNDROME 1 | (OMIM:211530) |
Congenital muscular dystrophy type 1B | (Orphanet:98893) |
Distal spinal muscular atrophy type 3 | (Orphanet:139547) |
FAZIO-LONDE DISEASE | (OMIM:211500) |
Glycogen storage disease due to acid maltase deficiency, infantile onset | (Orphanet:308552) |
Glycogen storage disease due to acid maltase deficiency, late-onset | (Orphanet:420429) |
Hereditary proximal myopathy with early respiratory failure | (Orphanet:178464) |
MYOPATHY, AREFLEXIA, RESPIRATORY DISTRESS, AND DYSPHAGIA, EARLY-ONSET | (OMIM:614399) |
Riboflavin transporter deficiency | (Orphanet:97229) |
SCAPULOPERONEAL SPINAL MUSCULAR ATROPHY | (OMIM:181405) |
SPINAL MUSCULAR ATROPHY, DISTAL, AUTOSOMAL RECESSIVE, 1 | (OMIM:604320) |