Abnormality of the sacroiliac joint

Symptom Information:

Symptom ID: HPO:0100781
Synonyms:
Sacroiliac joint anomaly [Orphanet:16750]
Sacroiliac joints anomalies [Orphanet:16750]
Quality:
Cross references:
Orphanet:16750 "Sacroiliac joints anomalies" [Orphanet:16750]
Is a (Direct Parents):
HPO         Abnormality of the ilium
Orphanet Abnormality of the vertebral column
HPO         Abnormality of the sacroiliac notch
HPO         Abnormality of the sacrum
Is a (Whole tree): HPO:
All(HPO:0000001)
    Phenotypic abnormality(HPO:0000118)
       Abnormality of the skeletal system(HPO:0000924)
          Abnormality of skeletal morphology(HPO:0011842)
             Abnormal joint morphology(HPO:0001367)
                Abnormality of lower limb joint(HPO:0100491)
                   Abnormality of the hip bone(HPO:0003272)
                      Abnormality of the ilium(HPO:0002867)
                         Abnormality of the sacroiliac joint(HPO:0100781)
             Abnormal appendicular skeleton morphology(HPO:0011844)
                Abnormality of pelvic girdle bone morphology(HPO:0002644)
                   Abnormality of the hip bone(HPO:0003272)
                      Abnormality of the ilium(HPO:0002867)
                         Abnormality of the sacroiliac joint(HPO:0100781)
                Abnormality of limb bone morphology(HPO:0002813)
                   Abnormality of the lower limb(HPO:0002814)
                      Abnormality of lower limb joint(HPO:0100491)
                         Abnormality of the hip bone(HPO:0003272)
                            Abnormality of the ilium(HPO:0002867)
                               Abnormality of the sacroiliac joint(HPO:0100781)
             Abnormal axial skeleton morphology(HPO:0009121)
                Abnormality of the vertebral column(HPO:0000925)
                   Abnormality of the sacrum(HPO:0005107)
                      Abnormality of the sacroiliac joint(HPO:0100781)
MedDRA:
Database Frequency: 6 / 7739
Resource:

All diseases associated with this symptom:

Chronic recurrent multifocal osteomyelitis (Orphanet:324964)
Juvenile idiopathic arthritis (Orphanet:92)
SAPHO syndrome (Orphanet:793)
TRAPS syndrome (Orphanet:32960)
Thanatophoric dysplasia (Orphanet:2655)
Thanatophoric dysplasia type 1 (Orphanet:1860)