Diaphragmatic paralysis

Symptom Information:

Symptom ID: HPO:0006597
Synonyms:
Paralysis of diaphragm (disorder) [Orphanet:32480]
Respiratory Paralysis [Orphanet:32480]
Diaphragmatic paralysis [OMIM:Diaphragmatic paralysis]
Diaphragmatic palsy [Orphanet:32480]
Respiratory paralysis [Orphanet:32480]
Diaphragmatic paralysis [Orphanet:32480]
Respiratory paralysis [MedDRA:10038708]
Diaphragmatic paralysis [MedDRA:10012725]
Paralysis of diaphragm [MedDRA:10012725]
Respiratory paralysis (HCP) [OMIM:Respiratory paralysis (HCP)]
Quality:
Cross references:
Orphanet:32480 "Diaphragmatic palsy" [Orphanet:32480]
OMIM: "Diaphragmatic paralysis" [OMIM:Diaphragmatic paralysis]
OMIM: "Respiratory paralysis (HCP)" [OMIM:Respiratory paralysis (HCP)]
UMLS:C0035232 "Respiratory Paralysis" [Orphanet:32480]
Is a (Direct Parents):
MedDRA Respiratory insufficiency
HPO         Diaphragmatic weakness
Orphanet Abnormality of the diaphragm
MedDRA Paralysis and paresis (excl cranial nerve)
Is a (Whole tree): HPO:
All(HPO:0000001)
    Phenotypic abnormality(HPO:0000118)
       Abnormality of the musculature(HPO:0003011)
          Abnormality of muscle physiology(HPO:0011804)
             Muscle weakness(HPO:0001324)
                Diaphragmatic weakness(HPO:0009113)
                   Diaphragmatic paralysis(HPO:0006597)
       Abnormality of the respiratory system(HPO:0002086)
          Abnormal respiratory system morphology(HPO:0012252)
             Abnormality of the diaphragm(HPO:0000775)
                Diaphragmatic weakness(HPO:0009113)
                   Diaphragmatic paralysis(HPO:0006597)
       Abnormality of the abdomen(HPO:0001438)
          Abnormality of the diaphragm(HPO:0000775)
             Diaphragmatic weakness(HPO:0009113)
                Diaphragmatic paralysis(HPO:0006597)
MedDRA:
Respiratory, thoracic and mediastinal disorders(MedDRA:10038738)
    Respiratory disorders NEC(MedDRA:10038716)
       Respiratory insufficiency(HPO:0002093)
          Diaphragmatic paralysis(HPO:0006597)
Nervous system disorders(MedDRA:10029205)
    Abnormality of movement(HPO:0100022)
       Paralysis and paresis (excl cranial nerve)(MedDRA:10033800)
          Diaphragmatic paralysis(HPO:0006597)
Database Frequency: 16 / 7739
Resource:

All diseases associated with this symptom:

Acute intermittent porphyria (Orphanet:79276)
Adult intestinal botulism (Orphanet:178487)
Botulism (Orphanet:1267)
Foodborne botulism (Orphanet:228371)
Glycogen storage disease due to acid maltase deficiency (Orphanet:365)
Hereditary coproporphyria (Orphanet:79273)
Iatrogenic botulism (Orphanet:254509)
MYOPATHY, AREFLEXIA, RESPIRATORY DISTRESS, AND DYSPHAGIA, EARLY-ONSET (OMIM:614399)
Muscular dystrophy, Selcen type (Orphanet:199340)
SPINAL MUSCULAR ATROPHY, DISTAL, AUTOSOMAL RECESSIVE, 1 (OMIM:604320)
Spinal muscular atrophy with respiratory distress (Orphanet:98920)
Thymic carcinoma (Orphanet:99868)
Thymic epithelial neoplasm (Orphanet:3398)
Thymic tumor (Orphanet:100100)
Toxin-mediated infectious botulism (Orphanet:230800)
Wound botulism (Orphanet:178475)