Multiple prenatal fractures

Symptom Information:

Symptom ID: HPO:0005855
Synonyms:
Congenital bone fractures [HPO:0005855]
Multiple fractures present at birth [HPO:0005855]
Multiple fractures, present at birth [HPO:0005855]
Numerous multiple fractures present at birth [HPO:0005855]
Numerous multiple fractures that are present at birth [HPO:0005855]
Congenital bone fractures [OMIM:Congenital bone fractures]
Multiple fractures present at birth [OMIM:Multiple fractures present at birth]
Multiple fractures, present at birth [OMIM:Multiple fractures, present at birth]
Multiple prenatal fractures [OMIM:Multiple prenatal fractures]
Numerous multiple fractures present at birth [OMIM:Numerous multiple fractures present at birth]
Numerous multiple fractures that are present at birth [OMIM:Numerous multiple fractures that are present at birth]
Quality:
Cross references:
OMIM: "Congenital bone fractures" [OMIM:Congenital bone fractures]
OMIM: "Multiple fractures present at birth" [OMIM:Multiple fractures present at birth]
OMIM: "Multiple fractures, present at birth" [OMIM:Multiple fractures, present at birth]
OMIM: "Multiple prenatal fractures" [OMIM:Multiple prenatal fractures]
OMIM: "Numerous multiple fractures present at birth" [OMIM:Numerous multiple fractures present at birth]
OMIM: "Numerous multiple fractures that are present at birth" [OMIM:Numerous multiple fractures that are present at birth]
Is a (Direct Parents):
HPO         Increased susceptibility to fractures
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:
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)