Hypoplastic iliac body

Symptom Information:

Symptom ID: HPO:0008824
Synonyms:
Hypoplastic iliac bodies [HPO:0008824]
Small iliac bodies [HPO:0008824]
Hypoplastic iliac body [OMIM:Hypoplastic iliac body]
Small iliac bodies [OMIM:Small iliac bodies]
Quality:
Cross references:
OMIM: "Hypoplastic iliac body" [OMIM:Hypoplastic iliac body]
OMIM: "Small iliac bodies" [OMIM:Small iliac bodies]
Is a (Direct Parents):
HPO         Hypoplastic ilia
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)
                         Hypoplastic ilia(HPO:0000946)
                            Hypoplastic iliac body(HPO:0008824)
             Abnormal appendicular skeleton morphology(HPO:0011844)
                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)
                               Hypoplastic ilia(HPO:0000946)
                                  Hypoplastic iliac body(HPO:0008824)
                Abnormality of pelvic girdle bone morphology(HPO:0002644)
                   Abnormality of the hip bone(HPO:0003272)
                      Abnormality of the ilium(HPO:0002867)
                         Hypoplastic ilia(HPO:0000946)
                            Hypoplastic iliac body(HPO:0008824)
MedDRA:
Database Frequency: 3 / 7739
Resource:

All diseases associated with this symptom:

Boomerang dysplasia (Orphanet:1263)
Spondyloepimetaphyseal dysplasia with joint laxity (Orphanet:93359)
Stüve-Wiedemann syndrome (Orphanet:3206)