Autophagic vacuoles

Symptom Information:

Symptom ID: HPO:0003736
Synonyms:
Autophagic vacuoles [OMIM:Autophagic vacuoles]
Quality:
Cross references:
OMIM: "Autophagic vacuoles" [OMIM:Autophagic vacuoles]
Is a (Direct Parents):
HPO         Abnormality of muscle fibers
Is a (Whole tree): HPO:
All(HPO:0000001)
    Phenotypic abnormality(HPO:0000118)
       Abnormality of the musculature(HPO:0003011)
          Abnormality of muscle morphology(HPO:0011805)
             Abnormality of muscle fibers(HPO:0004303)
                Autophagic vacuoles(HPO:0003736)
MedDRA:
Database Frequency: 5 / 7739
Resource:

All diseases associated with this symptom:

Alpha-crystallinopathy (Orphanet:98910)
Autosomal dominant limb-girdle muscular dystrophy type 1F (Orphanet:55595)
Glycogen storage disease due to LAMP-2 deficiency (Orphanet:34587)
MYOPATHY, AUTOPHAGIC VACUOLAR, INFANTILE-ONSET (OMIM:609500)
ZASP-related myofibrillar myopathy (Orphanet:98912)