Shallow acetabular fossae
Symptom Information:
Symptom ID: | HPO:0003182 | ||||||||||
Synonyms: |
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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 joint morphology(HPO:0001367) Abnormality of lower limb joint(HPO:0100491) Abnormality of the hip bone(HPO:0003272) Abnormality of the hip joint(HPO:0001384) Abnormality of the acetabulum(HPO:0003170) Shallow acetabular fossae(HPO:0003182) 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 hip joint(HPO:0001384) Abnormality of the acetabulum(HPO:0003170) Shallow acetabular fossae(HPO:0003182) Abnormality of pelvic girdle bone morphology(HPO:0002644) Abnormality of the hip bone(HPO:0003272) Abnormality of the hip joint(HPO:0001384) Abnormality of the acetabulum(HPO:0003170) Shallow acetabular fossae(HPO:0003182) MedDRA: |
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Database Frequency: | 10 / 7739 | ||||||||||
Resource: |
All diseases associated with this symptom:
BRACHYPHALANGY, POLYDACTYLY, AND TIBIAL APLASIA/HYPOPLASIA | (OMIM:609945) |
Carpenter syndrome | (Orphanet:65759) |
Down syndrome | (Orphanet:870) |
Hip dysplasia, Beukes type | (Orphanet:2114) |
Lowry-Wood syndrome | (Orphanet:1824) |
MUCOLIPIDOSIS III ALPHA/BETA | (OMIM:252600) |
Mucolipidosis type 3 | (Orphanet:577) |
Radio-ulnar synostosis - amegakaryocytic thrombocytopenia | (Orphanet:71289) |
Schimke immuno-osseous dysplasia | (Orphanet:1830) |
Singleton-Merten dysplasia | (Orphanet:85191) |