Trismus

Symptom Information:

Symptom ID: HPO:0000211
Synonyms:
Trismus (finding) [Orphanet:44200]
Trismus [Orphanet:44200]
Trismus [OMIM:Trismus]
Contractures/cramps/trismus/tetania/claudication/opisthotonos [Orphanet:44200]
Trismus [MedDRA:10044684]
Jaw cramp [MedDRA:10044684]
Jaw movements disturbance [MedDRA:10044684]
Jaw spasm [MedDRA:10044684]
Lockjaw [MedDRA:10044684]
Rigidity masticatory [MedDRA:10044684]
Spasm temporomandibular [MedDRA:10044684]
Trismus (rare) [OMIM:Trismus (rare)]
Muscle spasms [MedDRA:10028334]
Muscle contracture [Orphanet:44200]
Contracture (morphologic abnormality) [Orphanet:44200]
Spasm (finding) [Orphanet:44200]
Muscle contracture (disorder) [Orphanet:44200]
Contracture [Orphanet:44200]
Spasm [Orphanet:44200]
Quality:
Cross references:
Orphanet:44200 "Contractures/cramps/trismus/tetania/claudication/opisthotonos" [Orphanet:44200]
OMIM: "Trismus" [OMIM:Trismus]
OMIM: "Trismus (rare)" [OMIM:Trismus (rare)]
UMLS:C0041105 "Trismus" [HPO:0000211]
UMLS:C0041105 "Trismus" [Orphanet:44200]
UMLS:C0009917 "Contracture" [Orphanet:44200]
UMLS:C0037763 "Spasm" [Orphanet:44200]
Is a (Direct Parents):
MedDRA Muscle tone abnormalities
HPO         Abnormality of the mandible
Orphanet Muscle anomalies
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 skull(HPO:0000929)
                Abnormality of facial skeleton(HPO:0011821)
                   Abnormality of the mandible(HPO:0000277)
                      Trismus(HPO:0000211)
       Abnormality of the skeletal system(HPO:0000924)
          Abnormality of skeletal morphology(HPO:0011842)
             Abnormal axial skeleton morphology(HPO:0009121)
                Abnormality of the skull(HPO:0000929)
                   Abnormality of facial skeleton(HPO:0011821)
                      Abnormality of the mandible(HPO:0000277)
                         Trismus(HPO:0000211)
MedDRA:
Musculoskeletal and connective tissue disorders(MedDRA:10028395)
    Muscle disorders(MedDRA:10028302)
       Muscle tone abnormalities(MedDRA:10028343)
          Trismus(HPO:0000211)
Database Frequency: 9 / 7739
Resource:

All diseases associated with this symptom:

Autosomal recessive facio-digito-genital syndrome (Orphanet:1974)
Branchiogenic deafness syndrome (Orphanet:50815)
Buschke-Ollendorff syndrome (Orphanet:1306)
Carney complex-trismus-pseudocamptodactyly syndrome (Orphanet:319340)
Digitotalar dysmorphism (Orphanet:1146)
Gaucher disease type 2 (Orphanet:77260)
MELAS (Orphanet:550)
Nager syndrome (Orphanet:245)
Trismus - pseudocamptodactyly (Orphanet:3377)