Short sacroiliac notch

Symptom Information:

Symptom ID: HPO:0003185
Synonyms:
Shortened sacroiliac notches [HPO:0003185]
Shortened sacroiliac notches [OMIM:Shortened sacroiliac notches]
Small sacroiliac notches [OMIM:Small sacroiliac notches]
Quality:
Cross references:
OMIM: "Shortened sacroiliac notches" [OMIM:Shortened sacroiliac notches]
OMIM: "Small sacroiliac notches" [OMIM:Small sacroiliac notches]
Is a (Direct Parents):
HPO         Abnormality of the sacrum
HPO         Abnormality of the ilium
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 axial skeleton morphology(HPO:0009121)
                Abnormality of the vertebral column(HPO:0000925)
                   Abnormality of the sacrum(HPO:0005107)
                      Short sacroiliac notch(HPO:0003185)
             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)
                         Short sacroiliac notch(HPO:0003185)
             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)
                         Short sacroiliac notch(HPO:0003185)
                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)
                               Short sacroiliac notch(HPO:0003185)
MedDRA:
Database Frequency: 7 / 7739
Resource:

All diseases associated with this symptom:

Atelosteogenesis type II (Orphanet:56304)
Severe achondroplasia - developmental delay - acanthosis nigricans (Orphanet:85165)
Simpson-Golabi-Behmel syndrome (Orphanet:373)
Spondyloepiphyseal dysplasia tarda, Kohn type (Orphanet:163665)
Spondylometaphyseal dysplasia, Schmidt type (Orphanet:93316)
THANATOPHORIC DYSPLASIA, TYPE II (OMIM:187601)
Thanatophoric dysplasia type 1 (Orphanet:1860)