Multiple prenatal fractures
Symptom Information:
Symptom ID: | HPO:0005855 | |||||||||||
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 physiology(HPO:0011843) Increased susceptibility to fractures(HPO:0002659) Multiple prenatal fractures(HPO:0005855) MedDRA: |
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Database Frequency: | 10 / 7739 | |||||||||||
Resource: |
All diseases associated with this symptom:
Congenital osteogenesis imperfecta - microcephaly - cataracts | (Orphanet:2772) |
Greenberg dysplasia | (Orphanet:1426) |
OSTEOGENESIS IMPERFECTA, TYPE II | (OMIM:166210) |
OSTEOGENESIS IMPERFECTA, TYPE III | (OMIM:259420) |
OSTEOGENESIS IMPERFECTA, TYPE IX | (OMIM:259440) |
OSTEOGENESIS IMPERFECTA, TYPE VII | (OMIM:610682) |
OSTEOGENESIS IMPERFECTA, TYPE VIII | (OMIM:610915) |
Osteogenesis imperfecta type 2 | (Orphanet:216804) |
Osteogenesis imperfecta type 3 | (Orphanet:216812) |
SPINAL MUSCULAR ATROPHY, TYPE I, WITH CONGENITAL BONE FRACTURES | (OMIM:271225) |