Hip contracture
Symptom Information:
Symptom ID: | HPO:0003273 | |||||||||||
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 musculature(HPO:0003011) Abnormality of muscle morphology(HPO:0011805) Flexion contracture(HPO:0001371) Limb joint contracture(HPO:0003121) Contractures of the joints of the lower limbs(HPO:0005750) Hip contracture(HPO:0003273) Abnormality of connective tissue(HPO:0003549) Flexion contracture(HPO:0001371) Limb joint contracture(HPO:0003121) Contractures of the joints of the lower limbs(HPO:0005750) Hip contracture(HPO:0003273) Abnormality of the skeletal system(HPO:0000924) Abnormality of skeletal morphology(HPO:0011842) Abnormal joint morphology(HPO:0001367) Abnormality of joint mobility(HPO:0011729) Flexion contracture(HPO:0001371) Limb joint contracture(HPO:0003121) Contractures of the joints of the lower limbs(HPO:0005750) Hip contracture(HPO:0003273) Limitation of joint mobility(HPO:0001376) Limited hip movement(HPO:0008800) Hip contracture(HPO:0003273) Abnormal appendicular skeleton morphology(HPO:0011844) Abnormality of pelvic girdle bone morphology(HPO:0002644) Limited hip movement(HPO:0008800) Hip contracture(HPO:0003273) MedDRA: |
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Database Frequency: | 30 / 7739 | |||||||||||
Resource: |
All diseases associated with this symptom:
ARTHROGRYPOSIS, CONGENITAL, LOWER LIMB, X-LINKED | (OMIM:300158) |
ARTHROGRYPOSIS, DISTAL, TYPE 1A | (OMIM:108120) |
ARTHROGRYPOSIS, DISTAL, TYPE 2A | (OMIM:193700) |
Autosomal dominant childhood-onset proximal spinal muscular atrophy with contractures | (Orphanet:363454) |
Autosomal dominant chondrodysplasia punctata | (Orphanet:79344) |
Autosomal dominant congenital benign spinal muscular atrophy | (Orphanet:1216) |
Autosomal dominant multiple pterygium syndrome | (Orphanet:65743) |
Bruck syndrome | (Orphanet:2771) |
CONGENITAL CONTRACTURES OF THE LIMBS AND FACE, HYPOTONIA, AND DEVELOPMENTALDELAY | (OMIM:616266) |
Congenital contractural arachnodactyly | (Orphanet:115) |
Diastrophic dwarfism | (Orphanet:628) |
Digitotalar dysmorphism | (Orphanet:1146) |
Dyssegmental dysplasia - glaucoma | (Orphanet:1804) |
Freeman-Sheldon syndrome | (Orphanet:2053) |
Genitopatellar syndrome | (Orphanet:85201) |
Intellectual deficit - cataracts - calcified pinnae - myopathy | (Orphanet:3042) |
Kniest dysplasia | (Orphanet:485) |
MICROCEPHALIC OSTEODYSPLASTIC PRIMORDIAL DWARFISM, TYPE I | (OMIM:210710) |
MICROCEPHALIC OSTEODYSPLASTIC PRIMORDIAL DWARFISM, TYPE III | (OMIM:210730) |
MYOPATHY, CENTRONUCLEAR, 5 | (OMIM:615959) |
Metaphyseal chondrodysplasia, Jansen type | (Orphanet:33067) |
Microcephalic osteodysplastic primordial dwarfism types 1 and 3 | (Orphanet:2636) |
NEMALINE MYOPATHY 5 | (OMIM:605355) |
OTOONYCHOPERONEAL SYNDROME | (OMIM:259780) |
PROTRUSIO ACETABULI | (OMIM:177050) |
Roifman syndrome | (Orphanet:353298) |
SC PHOCOMELIA SYNDROME | (OMIM:269000) |
Schwartz-Jampel syndrome | (Orphanet:800) |
Spondylometaphyseal dysplasia, Golden type | (Orphanet:168544) |
Torg-Winchester syndrome | (Orphanet:3460) |