Iliac crest serration

Symptom Information:

Symptom ID: HPO:0008786
Synonyms:
Irregular lacy iliac crest [HPO:0008786]
Lacy appearance of iliac crest [HPO:0008786]
Irregular lacy iliac crest [OMIM:Irregular lacy iliac crest]
Irregular, lacy iliac crests [OMIM:Irregular, lacy iliac crests]
Quality:
Cross references:
OMIM: "Irregular lacy iliac crest" [OMIM:Irregular lacy iliac crest]
OMIM: "Irregular, lacy iliac crests" [OMIM:Irregular, lacy iliac crests]
Is a (Direct Parents):
HPO         Irregular iliac crest
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)
                         Irregular iliac crest(HPO:0003796)
                            Iliac crest serration(HPO:0008786)
             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)
                         Irregular iliac crest(HPO:0003796)
                            Iliac crest serration(HPO:0008786)
                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)
                               Irregular iliac crest(HPO:0003796)
                                  Iliac crest serration(HPO:0008786)
MedDRA:
Database Frequency: 4 / 7739
Resource:

All diseases associated with this symptom:

DYGGVE-MELCHIOR-CLAUSEN DISEASE (OMIM:223800)
Dyggve-Melchior-Clausen disease (Orphanet:239)
SPONDYLOMETAPHYSEAL DYSPLASIA, MEGARBANE-DAGHER-MELKI TYPE (OMIM:613320)
Spondylometaphyseal dysplasia, Sedaghatian type (Orphanet:93317)