Abnormality of pelvic girdle bone morphology

Symptom Information:

Symptom ID: HPO:0002644
Synonyms:
Abnormality of the pelvic girdle [HPO:0002644]
Pelvis anomaly [Orphanet:16570]
Congenital anomaly of pelvic bones (disorder) [Orphanet:16570]
Congenital anomaly of pelvic bones [Orphanet:16570]
Pelvis anomaly/Narrow/broad iliac wings/pubis abnormality [Orphanet:16570]
Broad iliac wing [Orphanet:16570]
Broad iliac wing [OMIM:Broad iliac wing]
Broad iliac wings [OMIM:Broad iliac wings]
Quality:
Cross references:
Orphanet:16570 "Pelvis anomaly/Narrow/broad iliac wings/pubis abnormality" [Orphanet:16570]
OMIM: "Broad iliac wing" [OMIM:Broad iliac wing]
OMIM: "Broad iliac wings" [OMIM:Broad iliac wings]
UMLS:C0685650 "Congenital anomaly of pelvic bones" [Orphanet:16570]
Is a (Direct Parents):
Orphanet Abnormality of the vertebral column
HPO         Abnormal appendicular skeleton morphology
HPO         Abnormal pelvis bone morphology
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:
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)