Multiple joint contractures
Symptom Information:
Symptom ID: | HPO:0002828 | ||
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 connective tissue(HPO:0003549) Flexion contracture(HPO:0001371) Multiple joint contractures(HPO:0002828) 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) MedDRA: |
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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) |