Trismus
Symptom Information:
Symptom ID: | HPO:0000211 | |||||||||||||||||||
Synonyms: |
|
|||||||||||||||||||
Quality: | ||||||||||||||||||||
Cross references: |
|
|||||||||||||||||||
Is a (Direct Parents): |
|
|||||||||||||||||||
Is a (Whole tree): |
HPO:
All(HPO:0000001) Phenotypic abnormality(HPO:0000118) 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) 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) 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) |