Sagittal craniosynostosis
Symptom Information:
Symptom ID: | HPO:0004442 | |||||||
Synonyms: |
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Cross references: |
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Is a (Direct Parents): |
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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 the calvaria(HPO:0002683) Abnormality of the fontanelles or cranial sutures(HPO:0000235) Abnormality of cranial sutures(HPO:0011329) Craniosynostosis(HPO:0001363) Sagittal craniosynostosis(HPO:0004442) Abnormality of calvarial morphology(HPO:0002648) Craniosynostosis(HPO:0001363) Sagittal craniosynostosis(HPO:0004442) 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) Sagittal craniosynostosis(HPO:0004442) Abnormality of calvarial morphology(HPO:0002648) Craniosynostosis(HPO:0001363) Sagittal craniosynostosis(HPO:0004442) MedDRA: |
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Database Frequency: | 16 / 7739 | |||||||
Resource: |
All diseases associated with this symptom:
Baller-Gerold syndrome | (Orphanet:1225) |
Cardiocranial syndrome, Pfeiffer type | (Orphanet:2872) |
Carpenter syndrome | (Orphanet:65759) |
Cranioectodermal dysplasia | (Orphanet:1515) |
Cranioectodermal dysplasia 1 | (OMIM:218330) |
Cranioectodermal dysplasia 3 | (OMIM:614099) |
Cranioectodermal dysplasia 4 | (OMIM:614378) |
Craniosynostosis - Dandy-Walker malformation - hydrocephalus | (Orphanet:1538) |
Craniosynostosis - anal anomalies - porokeratosis | (Orphanet:85199) |
Craniosynostosis and dental anomalies | (Orphanet:284149) |
Craniosynostosis, Philadelphia type | (Orphanet:1527) |
Crouzon disease | (Orphanet:207) |
Hurler syndrome | (Orphanet:93473) |
Hurler-Scheie syndrome | (Orphanet:93476) |
NOONAN SYNDROME 3 | (OMIM:609942) |
Trigonocephaly - short stature - developmental delay | (Orphanet:3369) |