Intermittent episodes of respiratory insufficiency due to muscle weakness

Symptom Information:

Symptom ID: HPO:0004889
Synonyms:
Intermittent episodes of respiratory insufficiency due to muscle weakness [OMIM:Intermittent episodes of respiratory insufficiency due to muscle weakness]
Quality:
Cross references:
OMIM: "Intermittent episodes of respiratory insufficiency due to muscle weakness" [OMIM:Intermittent episodes of respiratory insufficiency due to muscle weakness]
Is a (Direct Parents):
HPO         Respiratory insufficiency due to muscle weakness
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)
                      Intermittent episodes of respiratory insufficiency due to muscle weakness(HPO:0004889)
          Functional respiratory abnormality(HPO:0002795)
             Respiratory insufficiency(HPO:0002093)
                Respiratory insufficiency due to muscle weakness(HPO:0002747)
                   Intermittent episodes of respiratory insufficiency due to muscle weakness(HPO:0004889)
             Weakness of muscles of respiration(HPO:0004347)
                Respiratory insufficiency due to muscle weakness(HPO:0002747)
                   Intermittent episodes of respiratory insufficiency due to muscle weakness(HPO:0004889)
       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)
                      Intermittent episodes of respiratory insufficiency due to muscle weakness(HPO:0004889)
MedDRA:
Database Frequency: 1 / 7739
Resource:

All diseases associated with this symptom:

MYASTHENIC SYNDROME, CONGENITAL, 1A, SLOW-CHANNEL (OMIM:601462)