Limitation of joint mobility

Symptom Information:

Symptom ID: HPO:0001376
Synonyms:
Decreased joint mobility [HPO:0001376]
Decreased mobility of joints [HPO:0001376]
Limited joint mobility [HPO:0001376]
Limited joint motion [HPO:0001376]
Decreased joint mobility [OMIM:Decreased joint mobility]
Limitation of joint mobility [OMIM:Limitation of joint mobility]
Limited joint mobility [OMIM:Limited joint mobility]
Limited joint motion [OMIM:Limited joint motion]
Joint mobility decreased (rare) [OMIM:Joint mobility decreased (rare)]
Quality:
Cross references:
OMIM: "Decreased joint mobility" [OMIM:Decreased joint mobility]
OMIM: "Limitation of joint mobility" [OMIM:Limitation of joint mobility]
OMIM: "Limited joint mobility" [OMIM:Limited joint mobility]
OMIM: "Limited joint motion" [OMIM:Limited joint motion]
OMIM: "Joint mobility decreased (rare)" [OMIM:Joint mobility decreased (rare)]
Is a (Direct Parents):
HPO         Abnormality of joint mobility
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 joint morphology(HPO:0001367)
                Abnormality of joint mobility(HPO:0011729)
                   Limitation of joint mobility(HPO:0001376)
MedDRA:
Database Frequency: 27 / 7739
Resource:

All diseases associated with this symptom:

17q12 microdeletion syndrome (Orphanet:261265)
Atherosclerosis - deafness - diabetes - epilepsy - nephropathy (Orphanet:1192)
COCKAYNE SYNDROME A (OMIM:216400)
Cardiomyopathy-cataract-hip spine disease (Orphanet:1345)
Classical homocystinuria (Orphanet:394)
Cockayne syndrome (Orphanet:191)
Cranio-osteoarthropathy (Orphanet:1525)
Dyssegmental dysplasia, Rolland-Desbuquois type (Orphanet:156731)
FASCIAL DYSTROPHY, CONGENITAL (OMIM:228020)
GELEOPHYSIC DYSPLASIA 2 (OMIM:614185)
Hemochromatosis type 4 (Orphanet:139491)
Hurler syndrome (Orphanet:93473)
Hurler-Scheie syndrome (Orphanet:93476)
Kniest dysplasia (Orphanet:485)
Kyphomelic dysplasia (Orphanet:1801)
Leri pleonosteosis (Orphanet:2900)
Limited systemic sclerosis (Orphanet:220407)
Marden-Walker syndrome (Orphanet:2461)
Mucopolysaccharidosis type 2 (Orphanet:580)
Mucopolysaccharidosis type 2, severe form (Orphanet:217085)
Myhre syndrome (Orphanet:2588)
SPONDYLOEPIPHYSEAL DYSPLASIA TARDA, X-LINKED (OMIM:313400)
STIFF SKIN SYNDROME (OMIM:184900)
Scheie syndrome (Orphanet:93474)
Stiff skin syndrome (Orphanet:2833)
Werner syndrome (Orphanet:902)
Wolfram syndrome (Orphanet:3463)