Abnormality of pelvic girdle bone morphology
Symptom Information:
Symptom ID: | HPO:0002644 | ||||||||
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) MedDRA: |
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Database Frequency: | 31 / 7739 | ||||||||
Resource: |
All diseases associated with this symptom:
AREDYLD syndrome | (Orphanet:1133) |
Albers-Schönberg osteopetrosis | (Orphanet:53) |
Autosomal dominant osteopetrosis type 1 | (Orphanet:2783) |
Autosomal dominant osteosclerosis, Worth type | (Orphanet:2790) |
Autosomal dominant spastic paraplegia type 9 | (Orphanet:100990) |
Bladder exstrophy | (Orphanet:93930) |
Cartilage-hair hypoplasia | (Orphanet:175) |
Craniometaphyseal dysplasia | (Orphanet:1522) |
Ear-patella-short stature syndrome | (Orphanet:2554) |
Fetal akinesia deformation sequence | (Orphanet:994) |
Fucosidosis | (Orphanet:349) |
Hypochondroplasia | (Orphanet:429) |
Inclusion body myopathy with Paget disease of bone and frontotemporal dementia | (Orphanet:52430) |
METAPHYSEAL DYSPLASIA WITHOUT HYPOTRICHOSIS | (OMIM:250460) |
Moebius syndrome | (Orphanet:570) |
OSTEOARTHRITIS SUSCEPTIBILITY 1 | (OMIM:165720) |
OSTEODYSPLASTY, PRECOCIOUS, OF DANKS, MAYNE, AND KOZLOWSKI | (OMIM:259270) |
Osteogenesis imperfecta type 2 | (Orphanet:216804) |
Osteogenesis imperfecta type 5 | (Orphanet:216828) |
PAGET DISEASE OF BONE | (OMIM:602080) |
Pycnodysostosis | (Orphanet:763) |
Rhizomelic chondrodysplasia punctata type 2 | (Orphanet:309796) |
Saethre-Chotzen syndrome | (Orphanet:794) |
Sclerosteosis | (Orphanet:3152) |
Severe combined immunodeficiency due to adenosine deaminase deficiency | (Orphanet:277) |
Sillence syndrome | (Orphanet:3168) |
Spondylocarpotarsal synostosis | (Orphanet:3275) |
Weissenbacher- Zweymuller syndrome | (Orphanet:3450) |
Wolcott-Rallison syndrome | (Orphanet:1667) |
X-linked dominant chondrodysplasia punctata | (Orphanet:35173) |
X-linked hypophosphatemia | (Orphanet:89936) |