Pathologic fracture

Symptom Information:

Symptom ID: HPO:0002756
Synonyms:
PATHOLOGIC FRACTURES [HPO:0002756]
Spontaneous fracture [HPO:0002756]
SPONTANEOUS FRACTURES [HPO:0002756]
Pathologic fracture [OMIM:Pathologic fracture]
Pathologic fractures [OMIM:Pathologic fractures]
Spontaneous fracture [OMIM:Spontaneous fracture]
Spontaneous fractures [OMIM:Spontaneous fractures]
Pathologic fractures (hypophosphatasia only) [OMIM:Pathologic fractures (hypophosphatasia only)]
Spontaneous fracture (in older children) [OMIM:Spontaneous fracture (in older children)]
Quality:
Cross references:
OMIM: "Pathologic fracture" [OMIM:Pathologic fracture]
OMIM: "Pathologic fractures" [OMIM:Pathologic fractures]
OMIM: "Spontaneous fracture" [OMIM:Spontaneous fracture]
OMIM: "Spontaneous fractures" [OMIM:Spontaneous fractures]
OMIM: "Pathologic fractures (hypophosphatasia only)" [OMIM:Pathologic fractures (hypophosphatasia only)]
OMIM: "Spontaneous fracture (in older children)" [OMIM:Spontaneous fracture (in older children)]
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)
                Pathologic fracture(HPO:0002756)
MedDRA:
Database Frequency: 30 / 7739
Resource:

All diseases associated with this symptom:

Adult hypophosphatasia (Orphanet:247676)
Arthrogryposis - renal dysfunction - cholestasis (Orphanet:2697)
Aspartylglucosaminuria (Orphanet:93)
Autosomal dominant distal renal tubular acidosis (Orphanet:93608)
Autosomal recessive malignant osteopetrosis (Orphanet:667)
Blue rubber bleb nevus (Orphanet:1059)
Coats plus syndrome (Orphanet:313838)
Congenital erythropoietic porphyria (Orphanet:79277)
Connective tissue disorder due to lysyl hydroxylase-3 deficiency (Orphanet:300284)
Diaphyseal medullary stenosis - bone malignancy (Orphanet:85182)
Distal renal tubular acidosis (Orphanet:18)
Familial expansile osteolysis (Orphanet:85195)
Fibrous dysplasia of bone (Orphanet:249)
Gaucher disease type 1 (Orphanet:77259)
HAJDU-CHENEY SYNDROME (OMIM:102500)
Isolated glycerol kinase deficiency (Orphanet:408)
Lathosterolosis (Orphanet:46059)
McCune-Albright syndrome (Orphanet:562)
Metaphyseal chondrodysplasia, Jansen type (Orphanet:33067)
Mucolipidosis type 2 (Orphanet:576)
Nasu-Hakola disease (Orphanet:2770)
OSTEOPETROSIS, AUTOSOMAL RECESSIVE 1 (OMIM:259700)
Oculocerebrorenal syndrome (Orphanet:534)
Odontohypophosphatasia (Orphanet:247685)
Osteoporosis - pseudoglioma (Orphanet:2788)
Polyostotic fibrous dysplasia (Orphanet:93276)
Primary hyperoxaluria (Orphanet:416)
Primary hyperoxaluria type 1 (Orphanet:93598)
Spondyloepimetaphyseal dysplasia with joint laxity (Orphanet:93359)
Stüve-Wiedemann syndrome (Orphanet:3206)