Limitation of joint mobility
Symptom Information:
Symptom ID: | HPO:0001376 | |||||||||
Synonyms: |
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Quality: | ||||||||||
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 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: |
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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) |