Spinal rigidity
Symptom Information:
Symptom ID: | HPO:0003306 | |||||
Synonyms: |
|
|||||
Quality: | ||||||
Cross references: |
|
|||||
Is a (Direct Parents): |
|
|||||
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 axial skeleton morphology(HPO:0009121) Abnormality of the vertebral column(HPO:0000925) Spinal rigidity(HPO:0003306) MedDRA: |
|||||
Database Frequency: | 30 / 7739 | |||||
Resource: |
All diseases associated with this symptom:
Autosomal dominant limb-girdle muscular dystrophy type 1F | (Orphanet:55595) |
Autosomal recessive Emery-Dreifuss muscular dystrophy | (Orphanet:98855) |
Autosomal recessive limb-girdle muscular dystrophy type 2B | (Orphanet:268) |
Autosomal recessive limb-girdle muscular dystrophy type 2K | (Orphanet:86812) |
Autosomal recessive limb-girdle muscular dystrophy type 2M | (Orphanet:206554) |
Classic multiminicore myopathy | (Orphanet:324604) |
Congenital muscular dystrophy due to LMNA mutation | (Orphanet:157973) |
Congenital muscular dystrophy type 1B | (Orphanet:98893) |
Congenital muscular dystrophy, Ullrich type | (Orphanet:75840) |
Congenital myopathy with excess of thin filaments | (Orphanet:98904) |
Desmin-related myopathy with Mallory body-like inclusions | (Orphanet:84132) |
Emery-Dreifuss muscular dystrophy | (Orphanet:261) |
Fibrodysplasia ossificans progressiva | (Orphanet:337) |
Generalized congenital lipodystrophy with myopathy | (Orphanet:228429) |
Glycogen storage disease due to acid maltase deficiency, late-onset | (Orphanet:420429) |
MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH BRAIN AND EYEANOMALIES), TYPE A, 2 | (OMIM:613150) |
MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH BRAIN AND EYEANOMALIES), TYPE A, 4 | (OMIM:253800) |
MYOPATHY, REDUCING BODY, X-LINKED, CHILDHOOD-ONSET | (OMIM:300718) |
MYOPATHY, TUBULAR AGGREGATE, 2 | (OMIM:615883) |
Muscular dystrophy, Selcen type | (Orphanet:199340) |
Myosclerosis | (Orphanet:289380) |
NEMALINE MYOPATHY 2 | (OMIM:256030) |
Nemaline myopathy | (Orphanet:607) |
Progressive external ophthalmoplegia - myopathy - emaciation | (Orphanet:352447) |
Progressive non-infectious anterior vertebral fusion | (Orphanet:2062) |
Rigid spine syndrome | (Orphanet:97244) |
Schwartz-Jampel syndrome | (Orphanet:800) |
Steinert myotonic dystrophy | (Orphanet:273) |
X-linked Emery-Dreifuss muscular dystrophy | (Orphanet:98863) |
X-linked myopathy with postural muscle atrophy | (Orphanet:178461) |