Spinal rigidity

Symptom Information:

Symptom ID: HPO:0003306
Synonyms:
Rigid spine [HPO:0003306]
Rigid spine [Orphanet:16180]
Rigid spine [OMIM:Rigid spine]
Spinal rigidity [OMIM:Spinal rigidity]
Rigid spine (MEB) [OMIM:Rigid spine (MEB)]
Quality:
Cross references:
Orphanet:16180 "Rigid spine" [Orphanet:16180]
OMIM: "Rigid spine" [OMIM:Rigid spine]
OMIM: "Spinal rigidity" [OMIM:Spinal rigidity]
OMIM: "Rigid spine (MEB)" [OMIM:Rigid spine (MEB)]
Is a (Direct Parents):
Orphanet Abnormality of the vertebral column
HPO         Abnormality of the vertebral column
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)