Diaphragmatic weakness

Symptom Information:

Symptom ID: HPO:0009113
Synonyms:
Diaphragmatic paraparesis [HPO:0009113]
Diminished diaphragmatic motion [HPO:0009113]
Diaphragmatic paraparesis [OMIM:Diaphragmatic paraparesis]
Diaphragmatic weakness [OMIM:Diaphragmatic weakness]
Diminished diaphragmatic motion [OMIM:Diminished diaphragmatic motion]
Quality:
Cross references:
OMIM: "Diaphragmatic paraparesis" [OMIM:Diaphragmatic paraparesis]
OMIM: "Diaphragmatic weakness" [OMIM:Diaphragmatic weakness]
OMIM: "Diminished diaphragmatic motion" [OMIM:Diminished diaphragmatic motion]
Is a (Direct Parents):
HPO         Muscle weakness
HPO         Abnormality of the diaphragm
Is a (Whole tree): HPO:
All(HPO:0000001)
    Phenotypic abnormality(HPO:0000118)
       Abnormality of the respiratory system(HPO:0002086)
          Abnormal respiratory system morphology(HPO:0012252)
             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 abdomen(HPO:0001438)
          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)