Respiratory insufficiency due to muscle weakness
Symptom Information:
| Symptom ID: | HPO:0002747 | |||||||||||||
| Synonyms: |
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| 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) Weakness of muscles of respiration(HPO:0004347) Respiratory insufficiency due to muscle weakness(HPO:0002747) Abnormality of the respiratory system(HPO:0002086) Abnormal respiratory system morphology(HPO:0012252) Abnormality of lung morphology(HPO:0002088) Respiratory insufficiency(HPO:0002093) Respiratory insufficiency due to muscle weakness(HPO:0002747) Functional respiratory abnormality(HPO:0002795) Respiratory insufficiency(HPO:0002093) Respiratory insufficiency due to muscle weakness(HPO:0002747) Weakness of muscles of respiration(HPO:0004347) Respiratory insufficiency due to muscle weakness(HPO:0002747) MedDRA: Musculoskeletal and connective tissue disorders(MedDRA:10028395) Muscle disorders(MedDRA:10028302) Muscle weakness conditions(MedDRA:10062913) Respiratory insufficiency due to muscle weakness(HPO:0002747) |
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| Database Frequency: | 48 / 7739 | |||||||||||||
| Resource: |
All diseases associated with this symptom:
| AMYOTROPHIC LATERAL SCLEROSIS 10 WITH OR WITHOUT FRONTOTEMPORAL DEMENTIA | (OMIM:612069) |
| AMYOTROPHIC LATERAL SCLEROSIS 17 | (OMIM:614696) |
| AMYOTROPHIC LATERAL SCLEROSIS 19 | (OMIM:615515) |
| AMYOTROPHIC LATERAL SCLEROSIS 5 | (OMIM:602099) |
| Alpha-crystallinopathy | (Orphanet:98910) |
| Autosomal dominant limb-girdle muscular dystrophy type 1F | (Orphanet:55595) |
| Autosomal recessive centronuclear myopathy | (Orphanet:169186) |
| Autosomal recessive lower motor neuron disease with childhood onset | (Orphanet:206580) |
| Autosomal recessive progressive external ophthalmoplegia | (Orphanet:254886) |
| Bethlem myopathy | (Orphanet:610) |
| Combined immunodeficiency due to CRAC channel dysfunction | (Orphanet:169090) |
| Congenital fiber-type disproportion myopathy | (Orphanet:2020) |
| Congenital lethal myopathy, Compton-North type | (Orphanet:210163) |
| Congenital muscular dystrophy due to LMNA mutation | (Orphanet:157973) |
| Congenital muscular dystrophy type 1A | (Orphanet:258) |
| Congenital muscular dystrophy, Ullrich type | (Orphanet:75840) |
| Congenital myopathy with excess of thin filaments | (Orphanet:98904) |
| Desminopathy | (Orphanet:98909) |
| Distal myopathy with vocal cord weakness | (Orphanet:600) |
| Glycogen storage disease due to acid maltase deficiency | (Orphanet:365) |
| Hereditary myoclonus - progressive distal muscular atrophy | (Orphanet:2590) |
| Isolated cytochrome C oxidase deficiency | (Orphanet:254905) |
| MUSCULAR DYSTROPHY, CONGENITAL, MEROSIN-POSITIVE | (OMIM:609456) |
| MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH BRAIN AND EYEANOMALIES), TYPE A, 12 | (OMIM:615249) |
| MYASTHENIC SYNDROME, CONGENITAL, 10 | (OMIM:254300) |
| MYASTHENIC SYNDROME, CONGENITAL, 1B, FAST-CHANNEL | (OMIM:608930) |
| MYASTHENIC SYNDROME, CONGENITAL, 4A, SLOW-CHANNEL | (OMIM:605809) |
| MYASTHENIC SYNDROME, CONGENITAL, 4C, ASSOCIATED WITH ACETYLCHOLINERECEPTOR DEFICIENCY | (OMIM:608931) |
| MYOPATHY, CONGENITAL, WITH FIBER-TYPE DISPROPORTION | (OMIM:255310) |
| MYOPATHY, CONGENITAL, WITH FIBER-TYPE DISPROPORTION, X-LINKED | (OMIM:300580) |
| MYOPATHY, REDUCING BODY, X-LINKED, CHILDHOOD-ONSET | (OMIM:300718) |
| Mitochondrial DNA depletion syndrome, encephalomyopathic form with methylmalonic aciduria | (Orphanet:1933) |
| Mitochondrial DNA depletion syndrome, myopathic form | (Orphanet:254875) |
| Mitochondrial myopathy with reversible cytochrome C oxidase deficiency | (Orphanet:254864) |
| Myopathy, lactic acidosis, and sideroblastic anemia 2; MLASA2 | (OMIM:613561) |
| NEMALINE MYOPATHY 10 | (OMIM:616165) |
| NEMALINE MYOPATHY 2 | (OMIM:256030) |
| NEMALINE MYOPATHY 7 | (OMIM:610687) |
| Nemaline myopathy | (Orphanet:607) |
| Oculopharyngodistal myopathy | (Orphanet:98897) |
| Postsynaptic congenital myasthenic syndromes | (Orphanet:98913) |
| Presynaptic congenital myasthenic syndromes | (Orphanet:98914) |
| Reducing body myopathy | (Orphanet:97239) |
| Severe X-linked mitochondrial encephalomyopathy | (Orphanet:238329) |
| Steinert myotonic dystrophy | (Orphanet:273) |
| Synaptic congenital myasthenic syndromes | (Orphanet:98915) |
| Triose phosphate-isomerase deficiency | (Orphanet:868) |
| X-linked distal arthrogryposis multiplex congenita | (Orphanet:1145) |