Unicoronal synostosis

Symptom Information:

Symptom ID: HPO:0011315
Synonyms:
Quality:
Cross references:
Is a (Direct Parents):
HPO         Coronal craniosynostosis
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 the calvaria(HPO:0002683)
                      Abnormality of the fontanelles or cranial sutures(HPO:0000235)
                         Abnormality of cranial sutures(HPO:0011329)
                            Craniosynostosis(HPO:0001363)
                               Coronal craniosynostosis(HPO:0004440)
                                  Unicoronal synostosis(HPO:0011315)
                      Abnormality of calvarial morphology(HPO:0002648)
                         Craniosynostosis(HPO:0001363)
                            Coronal craniosynostosis(HPO:0004440)
                               Unicoronal synostosis(HPO:0011315)
       Abnormality of head or neck(HPO:0000152)
          Abnormality of the head(HPO:0000234)
             Abnormality of the skull(HPO:0000929)
                Abnormality of the calvaria(HPO:0002683)
                   Abnormality of the fontanelles or cranial sutures(HPO:0000235)
                      Abnormality of cranial sutures(HPO:0011329)
                         Craniosynostosis(HPO:0001363)
                            Coronal craniosynostosis(HPO:0004440)
                               Unicoronal synostosis(HPO:0011315)
                   Abnormality of calvarial morphology(HPO:0002648)
                      Craniosynostosis(HPO:0001363)
                         Coronal craniosynostosis(HPO:0004440)
                            Unicoronal synostosis(HPO:0011315)
MedDRA:
Database Frequency: 1 / 7739
Resource:

All diseases associated with this symptom:

Short-rib thoracic dysplasia 13 with or without polydactyly (OMIM:616300)