Decreased calvarial ossification
Symptom Information:
Symptom ID: | HPO:0005474 | ||||||||||
Synonyms: |
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Quality: | |||||||||||
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 skull ossification(HPO:0002703) Decreased skull ossification(HPO:0004331) Decreased calvarial ossification(HPO:0005474) Abnormality of the calvaria(HPO:0002683) Decreased calvarial ossification(HPO:0005474) 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 skull ossification(HPO:0002703) Decreased skull ossification(HPO:0004331) Decreased calvarial ossification(HPO:0005474) Abnormality of the calvaria(HPO:0002683) Decreased calvarial ossification(HPO:0005474) Abnormal bone structure(HPO:0003330) Abnormal bone ossification(HPO:0011849) Decreased skull ossification(HPO:0004331) Decreased calvarial ossification(HPO:0005474) MedDRA: |
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Database Frequency: | 8 / 7739 | ||||||||||
Resource: |
All diseases associated with this symptom:
Congenital osteogenesis imperfecta - microcephaly - cataracts | (Orphanet:2772) |
Lethal restrictive dermopathy | (Orphanet:1662) |
OSTEOGENESIS IMPERFECTA, TYPE II | (OMIM:166210) |
OSTEOGENESIS IMPERFECTA, TYPE III | (OMIM:259420) |
OSTEOGENESIS IMPERFECTA, TYPE VII | (OMIM:610682) |
Osteogenesis imperfecta type 3 | (Orphanet:216812) |
Perinatal lethal hypophosphatasia | (Orphanet:247623) |
Phocomelia, Schinzel type | (Orphanet:2879) |