Hip contracture

Symptom Information:

Symptom ID: HPO:0003273
Synonyms:
Flexion contracture of hips [HPO:0003273]
Flexion contractures of hips [HPO:0003273]
Hip contractures [HPO:0003273]
Hip flexion contractures [HPO:0003273]
Flexion contracture of hips [OMIM:Flexion contracture of hips]
Flexion contractures of hips [OMIM:Flexion contractures of hips]
Hip contracture [OMIM:Hip contracture]
Hip contractures [OMIM:Hip contractures]
Hip flexion contractures [OMIM:Hip flexion contractures]
Hip contractures (25%) [OMIM:Hip contractures (25%)]
Hip contractures (in some patients) [OMIM:Hip contractures (in some patients)]
Quality:
Cross references:
OMIM: "Flexion contracture of hips" [OMIM:Flexion contracture of hips]
OMIM: "Flexion contractures of hips" [OMIM:Flexion contractures of hips]
OMIM: "Hip contracture" [OMIM:Hip contracture]
OMIM: "Hip contractures" [OMIM:Hip contractures]
OMIM: "Hip flexion contractures" [OMIM:Hip flexion contractures]
OMIM: "Hip contractures (25%)" [OMIM:Hip contractures (25%)]
OMIM: "Hip contractures (in some patients)" [OMIM:Hip contractures (in some patients)]
Is a (Direct Parents):
HPO         Limited hip movement
HPO         Contractures of the joints of the lower limbs
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 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)
       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)
MedDRA:
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)