Respiratory insufficiency due to muscle weakness

Symptom Information:

Symptom ID: HPO:0002747
Synonyms:
Decreased respiratory function due to muscle weakness [HPO:0002747]
Respiratory distress due to muscle weakness [HPO:0002747]
Respiratory failure due to muscle weakness [HPO:0002747]
Respiratory muscle weakness [HPO:0002747]
Decreased respiratory function due to muscle weakness [OMIM:Decreased respiratory function due to muscle weakness]
Respiratory distress due to muscle weakness [OMIM:Respiratory distress due to muscle weakness]
Respiratory failure due to muscle weakness [OMIM:Respiratory failure due to muscle weakness]
Respiratory insufficiency due to muscle weakness [OMIM:Respiratory insufficiency due to muscle weakness]
Respiratory muscle weakness [OMIM:Respiratory muscle weakness]
Respiratory insufficiency due to muscle weakness (1 patient) [OMIM:Respiratory insufficiency due to muscle weakness (1 patient)]
Respiratory insufficiency due to muscle weakness (especially in infancy) [OMIM:Respiratory insufficiency due to muscle weakness (especially in infancy)]
Respiratory insufficiency due to muscle weakness (in some patients) [OMIM:Respiratory insufficiency due to muscle weakness (in some patients)]
Respiratory muscle weakness [MedDRA:10070833]
Quality:
Cross references:
OMIM: "Decreased respiratory function due to muscle weakness" [OMIM:Decreased respiratory function due to muscle weakness]
OMIM: "Respiratory distress due to muscle weakness" [OMIM:Respiratory distress due to muscle weakness]
OMIM: "Respiratory failure due to muscle weakness" [OMIM:Respiratory failure due to muscle weakness]
OMIM: "Respiratory insufficiency due to muscle weakness" [OMIM:Respiratory insufficiency due to muscle weakness]
OMIM: "Respiratory muscle weakness" [OMIM:Respiratory muscle weakness]
OMIM: "Respiratory insufficiency due to muscle weakness (1 patient)" [OMIM:Respiratory insufficiency due to muscle weakness (1 patient)]
OMIM: "Respiratory insufficiency due to muscle weakness (especially in infancy)" [OMIM:Respiratory insufficiency due to muscle weakness (especially in infancy)]
OMIM: "Respiratory insufficiency due to muscle weakness (in some patients)" [OMIM:Respiratory insufficiency due to muscle weakness (in some patients)]
Is a (Direct Parents):
HPO         Weakness of muscles of respiration
MedDRA Muscle weakness conditions
HPO         Respiratory insufficiency
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 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)
       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)
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)
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)