Narrow greater sacrosciatic notches
Symptom Information:
Symptom ID: | HPO:0003375 | |||||||||||||
Synonyms: |
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Cross references: |
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Is a (Direct Parents): |
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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: |
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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) |