Flat acetabular roof
Symptom Information:
Symptom ID: | HPO:0003180 | ||||||||||||
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 hip bone(HPO:0003272) Abnormality of the hip joint(HPO:0001384) Abnormality of the acetabulum(HPO:0003170) Flat acetabular roof(HPO:0003180) 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) Flat acetabular roof(HPO:0003180) 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) Flat acetabular roof(HPO:0003180) MedDRA: |
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Database Frequency: | 25 / 7739 | ||||||||||||
Resource: |
All diseases associated with this symptom:
Atelosteogenesis type II | (Orphanet:56304) |
Atelosteogenesis type III | (Orphanet:56305) |
BARATELA-SCOTT SYNDROME | (OMIM:300881) |
Brachyolmia type 1, Hobaek type | (Orphanet:93301) |
DESBUQUOIS DYSPLASIA 1 | (OMIM:251450) |
DYGGVE-MELCHIOR-CLAUSEN DISEASE | (OMIM:223800) |
Desbuquois syndrome | (Orphanet:1425) |
Dyggve-Melchior-Clausen disease | (Orphanet:239) |
Goldblatt syndrome | (Orphanet:166272) |
Kyphomelic dysplasia | (Orphanet:1801) |
Mucolipidosis type 2 | (Orphanet:576) |
Opsismodysplasia | (Orphanet:2746) |
Platyspondylic dysplasia, Torrance type | (Orphanet:85166) |
Pseudoleprechaunism syndrome, Patterson type | (Orphanet:2976) |
SPONDYLOMEGAEPIPHYSEAL DYSPLASIA WITH UPPER LIMB MESOMELIA, PUNCTATECALCIFICATIONS, AND DEAFNESS | (OMIM:609616) |
Schneckenbecken dysplasia | (Orphanet:3144) |
Short-rib thoracic dysplasia 13 with or without polydactyly | (OMIM:616300) |
Sillence syndrome | (Orphanet:3168) |
Spondyloepimetaphyseal dysplasia, Geneviève type | (Orphanet:168454) |
Spondyloepimetaphyseal dysplasia, matrilin-3 type | (Orphanet:156728) |
Spondylometaphyseal dysplasia, A4 type | (Orphanet:168555) |
Spondylometaphyseal dysplasia, Kozlowski type | (Orphanet:93314) |
Spondylometaphyseal dysplasia, Sedaghatian type | (Orphanet:93317) |
Spondyloperipheral dysplasia - short ulna | (Orphanet:1856) |
X-linked spondyloepimetaphyseal dysplasia | (Orphanet:93349) |