Fracture

Symptom Information:

Symptom ID: MedDRA:10017076
Synonyms:
Fracture [OMIM:Fracture]
Fractures [OMIM:Fractures]
Fractures (in some patients) [OMIM:Fractures (in some patients)]
Fractures (rare) [OMIM:Fractures (rare)]
Quality:
Cross references:
OMIM: "Fracture" [OMIM:Fracture]
OMIM: "Fractures" [OMIM:Fractures]
OMIM: "Fractures (in some patients)" [OMIM:Fractures (in some patients)]
OMIM: "Fractures (rare)" [OMIM:Fractures (rare)]
Is a (Direct Parents):
MedDRA Fractures NEC
Is a (Whole tree): HPO:
MedDRA:
Musculoskeletal and connective tissue disorders(MedDRA:10028395)
    Fractures(MedDRA:10017322)
       Fractures NEC(MedDRA:10072986)
          Fracture(MedDRA:10017076)
Database Frequency: 18 / 7739
Resource:

All diseases associated with this symptom:

Cerebrotendinous xanthomatosis (Orphanet:909)
Craniometadiaphyseal dysplasia, wormian bone type (Orphanet:85184)
Ehlers-Danlos syndrome type 7A (Orphanet:99875)
Ehlers-Danlos syndrome type 7B (Orphanet:99876)
Ehlers-Danlos syndrome, arthrochalasic type (Orphanet:1899)
Ehlers-Danlos syndrome, kyphoscoliotic and deafness type (Orphanet:300179)
HYPOGONADOTROPIC HYPOGONADISM 17 WITH OR WITHOUT ANOSMIA (OMIM:615266)
HYPOGONADOTROPIC HYPOGONADISM 18 WITH OR WITHOUT ANOSMIA (OMIM:615267)
HYPOGONADOTROPIC HYPOGONADISM 19 WITH OR WITHOUT ANOSMIA (OMIM:615269)
HYPOGONADOTROPIC HYPOGONADISM 20 WITH OR WITHOUT ANOSMIA (OMIM:615270)
HYPOGONADOTROPIC HYPOGONADISM 21 WITH OR WITHOUT ANOSMIA (OMIM:615271)
Infantile hypophosphatasia (Orphanet:247651)
Lethal multiple pterygium syndrome (Orphanet:33108)
Mohr-Tranebjaerg syndrome (Orphanet:52368)
Osteoglophonic dwarfism (Orphanet:2645)
Perinatal lethal hypophosphatasia (Orphanet:247623)
Pyle disease (Orphanet:3005)
X-linked lethal multiple pterygium syndrome (Orphanet:79447)