Facial paralysis

Symptom Information:

Symptom ID: HPO:0007209
Synonyms:
Facial paralysis [OMIM:Facial paralysis]
Quality:
Cross references:
OMIM: "Facial paralysis" [OMIM:Facial paralysis]
Is a (Direct Parents):
HPO         Abnormality of facial musculature
HPO         Cranial nerve compression
Is a (Whole tree): HPO:
All(HPO:0000001)
    Phenotypic abnormality(HPO:0000118)
       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)
                   Cranial nerve compression(HPO:0001293)
                      Facial paralysis(HPO:0007209)
       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 paralysis(HPO:0007209)
       Abnormality of the musculature(HPO:0003011)
          Abnormality of facial musculature(HPO:0000301)
             Facial paralysis(HPO:0007209)
MedDRA:
Database Frequency: 8 / 7739
Resource:

All diseases associated with this symptom:

Albers-Schönberg osteopetrosis (Orphanet:53)
Autosomal recessive malignant osteopetrosis (Orphanet:667)
Deafness - ear malformation - facial palsy (Orphanet:3232)
Dysosteosclerosis (Orphanet:1782)
OSTEOPETROSIS, AUTOSOMAL RECESSIVE 1 (OMIM:259700)
OSTEOPETROSIS, AUTOSOMAL RECESSIVE 2 (OMIM:259710)
Polyarteritis nodosa, childhood-onset (OMIM:615688)
Sneddon syndrome (Orphanet:820)