Multiple joint contractures

Symptom Information:

Symptom ID: HPO:0002828
Synonyms:
Multiple joint contractures [OMIM:Multiple joint contractures]
Quality:
Cross references:
OMIM: "Multiple joint contractures" [OMIM:Multiple joint contractures]
Is a (Direct Parents):
HPO         Flexion contracture
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)
                   Flexion contracture(HPO:0001371)
                      Multiple joint contractures(HPO:0002828)
       Abnormality of the musculature(HPO:0003011)
          Abnormality of muscle morphology(HPO:0011805)
             Flexion contracture(HPO:0001371)
                Multiple joint contractures(HPO:0002828)
       Abnormality of connective tissue(HPO:0003549)
          Flexion contracture(HPO:0001371)
             Multiple joint contractures(HPO:0002828)
MedDRA:
Database Frequency: 16 / 7739
Resource:

All diseases associated with this symptom:

CRANIOSYNOSTOSIS-MENTAL RETARDATION SYNDROME OF LIN AND GETTIG (OMIM:218649)
Fetal Gaucher disease (Orphanet:85212)
Hurler syndrome (Orphanet:93473)
Hurler-Scheie syndrome (Orphanet:93476)
MICROHYDRANENCEPHALY (OMIM:605013)
MYASTHENIC SYNDROME, CONGENITAL, 15 (OMIM:616227)
Marden-Walker syndrome (Orphanet:2461)
Morse-Rawnsley-Sargent syndrome (Orphanet:2570)
Mucopolysaccharidosis type 2 (Orphanet:580)
Mucopolysaccharidosis type 2, attenuated form (Orphanet:217093)
OPITZ-KAVEGGIA SYNDROME (OMIM:305450)
Scheie syndrome (Orphanet:93474)
Terminal osseous dysplasia - pigmentary defects (Orphanet:88630)
Timothy syndrome (Orphanet:65283)
X-linked distal arthrogryposis multiplex congenita (Orphanet:1145)
X-linked intellectual disability-cardiomegaly-congestive heart failure syndrome (Orphanet:324410)