Acetabular dysplasia

Symptom Information:

Symptom ID: HPO:0008807
Synonyms:
Dysplastic acetabulae [HPO:0008807]
Acetabular dysplasia [OMIM:Acetabular dysplasia]
Dysplastic acetabulae [OMIM:Dysplastic acetabulae]
Acetabular dysplasia (rare) [OMIM:Acetabular dysplasia (rare)]
Quality:
Cross references:
OMIM: "Acetabular dysplasia" [OMIM:Acetabular dysplasia]
OMIM: "Dysplastic acetabulae" [OMIM:Dysplastic acetabulae]
OMIM: "Acetabular dysplasia (rare)" [OMIM:Acetabular dysplasia (rare)]
Is a (Direct Parents):
HPO         Abnormality of the acetabulum
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 hip bone(HPO:0003272)
                      Abnormality of the hip joint(HPO:0001384)
                         Abnormality of the acetabulum(HPO:0003170)
                            Acetabular dysplasia(HPO:0008807)
                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)
                                  Acetabular dysplasia(HPO:0008807)
             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)
                            Acetabular dysplasia(HPO:0008807)
MedDRA:
Database Frequency: 6 / 7739
Resource:

All diseases associated with this symptom:

Acro-fronto-facio-nasal dysostosis (Orphanet:1784)
DEVELOPMENTAL DYSPLASIA OF THE HIP 1 (OMIM:142700)
Familial clubfoot due to 17q23.1q23.2 microduplication (Orphanet:238578)
Hermansky-Pudlak syndrome with neutropenia (Orphanet:183678)
Mucopolysaccharidosis type 7 (Orphanet:584)
Richieri Costa-Pereira syndrome (Orphanet:3102)