Calvarial hyperostosis
Symptom Information:
Symptom ID: | HPO:0004490 | |||||||
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 the skeletal system(HPO:0000924) Abnormality of skeletal morphology(HPO:0011842) Hyperostosis(HPO:0100774) Cranial hyperostosis(HPO:0004437) Calvarial hyperostosis(HPO:0004490) Abnormal axial skeleton morphology(HPO:0009121) Abnormality of the skull(HPO:0000929) Abnormality of the calvaria(HPO:0002683) Cranial hyperostosis(HPO:0004437) Calvarial hyperostosis(HPO:0004490) 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) Cranial hyperostosis(HPO:0004437) Calvarial hyperostosis(HPO:0004490) MedDRA: |
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Database Frequency: | 11 / 7739 | |||||||
Resource: |
All diseases associated with this symptom:
ACRODYSOSTOSIS 1 WITH OR WITHOUT HORMONE RESISTANCE | (OMIM:101800) |
AREDYLD syndrome | (Orphanet:1133) |
Acrodysostosis with multiple hormone resistance | (Orphanet:280651) |
CALVARIAL HYPEROSTOSIS | (OMIM:302030) |
Caffey disease | (Orphanet:1310) |
HYPEROSTOSIS CRANIALIS INTERNA | (OMIM:144755) |
Mucopolysaccharidosis type 1 | (Orphanet:579) |
Pancreatic insufficiency - anemia - hyperostosis | (Orphanet:199337) |
Proteus syndrome | (Orphanet:744) |
SCLEROSTEOSIS 1 | (OMIM:269500) |
Weismann-Netter syndrome | (Orphanet:3344) |