Generalized hypotonia due to defect at the neuromuscular junction

Symptom Information:

Symptom ID: HPO:0003397
Synonyms:
Generalized hypotonia due to defect at the neuromuscular junction [OMIM:Generalized hypotonia due to defect at the neuromuscular junction]
Quality:
Cross references:
OMIM: "Generalized hypotonia due to defect at the neuromuscular junction" [OMIM:Generalized hypotonia due to defect at the neuromuscular junction]
Is a (Direct Parents):
HPO         Abnormal synaptic transmission at the neuromuscular junction
HPO         Generalized hypotonia
Is a (Whole tree): HPO:
All(HPO:0000001)
    Phenotypic abnormality(HPO:0000118)
       Abnormality of the musculature(HPO:0003011)
          Abnormality of muscle physiology(HPO:0011804)
             Abnormal muscle tone(HPO:0003808)
                Muscular hypotonia(HPO:0001252)
                   Generalized hypotonia(HPO:0001290)
                      Generalized hypotonia due to defect at the neuromuscular junction(HPO:0003397)
       Abnormality of the nervous system(HPO:0000707)
          Abnormality of nervous system morphology(HPO:0012639)
             Abnormal peripheral nervous system morphology(HPO:0000759)
                Abnormal synaptic transmission at the neuromuscular junction(HPO:0003398)
                   Generalized hypotonia due to defect at the neuromuscular junction(HPO:0003397)
MedDRA:
Database Frequency: 2 / 7739
Resource:

All diseases associated with this symptom:

MYASTHENIC SYNDROME, CONGENITAL, 4A, SLOW-CHANNEL (OMIM:605809)
Presynaptic congenital myasthenic syndromes (Orphanet:98914)