Frontalis muscle weakness

Symptom Information:

Symptom ID: HPO:0004661
Synonyms:
Weak frontalis muscle [HPO:0004661]
Frontalis muscle weakness [OMIM:Frontalis muscle weakness]
Weak frontalis muscle [OMIM:Weak frontalis muscle]
Quality:
Cross references:
OMIM: "Frontalis muscle weakness" [OMIM:Frontalis muscle weakness]
OMIM: "Weak frontalis muscle" [OMIM:Weak frontalis muscle]
Is a (Direct Parents):
HPO         Facial palsy
Is a (Whole tree): HPO:
All(HPO:0000001)
    Phenotypic abnormality(HPO:0000118)
       Abnormality of the musculature(HPO:0003011)
          Abnormality of muscle physiology(HPO:0011804)
             Muscle weakness(HPO:0001324)
                Facial palsy(HPO:0010628)
                   Frontalis muscle weakness(HPO:0004661)
          Abnormality of facial musculature(HPO:0000301)
             Facial palsy(HPO:0010628)
                Frontalis muscle weakness(HPO:0004661)
       Abnormality of the nervous system(HPO:0000707)
          Abnormality of nervous system morphology(HPO:0012639)
             Morphological abnormality of the central nervous system(HPO:0002011)
                Abnormality of the cranial nerves(HPO:0001291)
                   Abnormality of the seventh cranial nerve(HPO:0010827)
                      Facial palsy(HPO:0010628)
                         Frontalis muscle weakness(HPO:0004661)
                   Cranial nerve paralysis(HPO:0006824)
                      Facial palsy(HPO:0010628)
                         Frontalis muscle weakness(HPO:0004661)
       Abnormality of head or neck(HPO:0000152)
          Abnormality of the head(HPO:0000234)
             Abnormality of the face(HPO:0000271)
                Abnormality of facial soft tissue(HPO:0011799)
                   Abnormality of facial musculature(HPO:0000301)
                      Facial palsy(HPO:0010628)
                         Frontalis muscle weakness(HPO:0004661)
MedDRA:
Database Frequency: 2 / 7739
Resource:

All diseases associated with this symptom:

Blepharophimosis - ptosis - esotropia - syndactyly - short stature (Orphanet:2057)
MYOPATHY, CONGENITAL, WITH FIBER-TYPE DISPROPORTION, X-LINKED (OMIM:300580)