Eyelid apraxia

Symptom Information:

Symptom ID: HPO:0000658
Synonyms:
Eyelid apraxia [OMIM:Eyelid apraxia]
Quality:
Cross references:
OMIM: "Eyelid apraxia" [OMIM:Eyelid apraxia]
Is a (Direct Parents):
HPO         Abnormality of the eyelid
HPO         Apraxia
Is a (Whole tree): HPO:
All(HPO:0000001)
    Phenotypic abnormality(HPO:0000118)
       Abnormality of head or neck(HPO:0000152)
          Abnormality of the head(HPO:0000234)
             Abnormality of the face(HPO:0000271)
                Abnormality of the periorbital region(HPO:0000606)
                   Abnormality of the eyelid(HPO:0000492)
                      Eyelid apraxia(HPO:0000658)
                obsolete Abnormality of the ocular region(HPO:0000284)
                   Abnormality of the eyelid(HPO:0000492)
                      Eyelid apraxia(HPO:0000658)
       Abnormality of the nervous system(HPO:0000707)
          Abnormality of nervous system physiology(HPO:0012638)
             Abnormality of higher mental function(HPO:0011446)
                Apraxia(HPO:0002186)
                   Eyelid apraxia(HPO:0000658)
             Abnormality of central motor function(HPO:0011442)
                Apraxia(HPO:0002186)
                   Eyelid apraxia(HPO:0000658)
MedDRA:
Database Frequency: 5 / 7739
Resource:

All diseases associated with this symptom:

Classical progressive supranuclear palsy (Orphanet:240071)
PARKINSON DISEASE 20, EARLY-ONSET (OMIM:615530)
Pantothenate kinase-associated neurodegeneration (Orphanet:157850)
SUPRANUCLEAR PALSY, PROGRESSIVE, 1 (OMIM:601104)
SUPRANUCLEAR PALSY, PROGRESSIVE, 2 (OMIM:609454)