Narrow greater sacrosciatic notches

Symptom Information:

Symptom ID: HPO:0003375
Synonyms:
Narrow sacrosciatic notch [HPO:0003375]
Narrow sciatic notches [HPO:0003375]
Narrowed greater sciatic notch [HPO:0003375]
Narrowed sacrosciatic notch [HPO:0003375]
Small sacrosciatic notch [HPO:0003375]
Small sacrosciatic notches [HPO:0003375]
Narrow sacrosciatic notch [OMIM:Narrow sacrosciatic notch]
Narrow sciatic notches [OMIM:Narrow sciatic notches]
Narrowed greater sciatic notch [OMIM:Narrowed greater sciatic notch]
Narrowed sacrosciatic notch [OMIM:Narrowed sacrosciatic notch]
Small sacrosciatic notch [OMIM:Small sacrosciatic notch]
Small sacrosciatic notches [OMIM:Small sacrosciatic notches]
Narrow sacrosciatic notches [OMIM:Narrow sacrosciatic notches]
Quality:
Cross references:
OMIM: "Narrow sacrosciatic notch" [OMIM:Narrow sacrosciatic notch]
OMIM: "Narrow sciatic notches" [OMIM:Narrow sciatic notches]
OMIM: "Narrowed greater sciatic notch" [OMIM:Narrowed greater sciatic notch]
OMIM: "Narrowed sacrosciatic notch" [OMIM:Narrowed sacrosciatic notch]
OMIM: "Small sacrosciatic notch" [OMIM:Small sacrosciatic notch]
OMIM: "Small sacrosciatic notches" [OMIM:Small sacrosciatic notches]
OMIM: "Narrow sacrosciatic notches" [OMIM:Narrow sacrosciatic notches]
Is a (Direct Parents):
HPO         Abnormality of the greater sacrosciatic notch
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 appendicular skeleton morphology(HPO:0011844)
                Abnormality of pelvic girdle bone morphology(HPO:0002644)
                   Abnormality of the greater sacrosciatic notch(HPO:0010456)
                      Narrow greater sacrosciatic notches(HPO:0003375)
MedDRA:
Database Frequency: 13 / 7739
Resource:

All diseases associated with this symptom:

Axial spondylometaphyseal dysplasia (Orphanet:168549)
DYGGVE-MELCHIOR-CLAUSEN DISEASE (OMIM:223800)
Dyggve-Melchior-Clausen disease (Orphanet:239)
Dyssegmental dysplasia, Rolland-Desbuquois type (Orphanet:156731)
FIBROCHONDROGENESIS 1 (OMIM:228520)
Fibrochondrogenesis (Orphanet:2021)
Mucopolysaccharidosis type 7 (Orphanet:584)
SPONDYLOMEGAEPIPHYSEAL DYSPLASIA WITH UPPER LIMB MESOMELIA, PUNCTATECALCIFICATIONS, AND DEAFNESS (OMIM:609616)
Spondyloepimetaphyseal dysplasia congenita, Strudwick type (Orphanet:93346)
Spondyloepimetaphyseal dysplasia, Shohat type (Orphanet:93352)
Spondylometaphyseal dysplasia - cone-rod dystrophy (Orphanet:85167)
Spondylometaphyseal dysplasia, A4 type (Orphanet:168555)
Spondylometaphyseal dysplasia, Sedaghatian type (Orphanet:93317)