Opisthotonus

Symptom Information:

Symptom ID: HPO:0002179
Synonyms:
Opisthotonos [HPO:0002179]
Opisthotonos [Orphanet:44200]
Opisthotonus (finding) [Orphanet:44200]
OPISTHOTONOS [HPO:0002179]
Opisthotonus [Orphanet:44200]
Opisthotonos [OMIM:Opisthotonos]
Opisthotonus [OMIM:Opisthotonus]
Contractures/cramps/trismus/tetania/claudication/opisthotonos [Orphanet:44200]
Opisthotonus [MedDRA:10030899]
Back arched backward [MedDRA:10030899]
Back arched backwards [MedDRA:10030899]
Episthotonos [MedDRA:10030899]
Opisthotonos [MedDRA:10030899]
Spine rigidly extended [MedDRA:10030899]
Trunk bowed back [MedDRA:10030899]
Opisthotonos (type II) [OMIM:Opisthotonos (type II)]
Muscle spasms [MedDRA:10028334]
Muscle contracture [Orphanet:44200]
Contracture (morphologic abnormality) [Orphanet:44200]
Spasm (finding) [Orphanet:44200]
Muscle contracture (disorder) [Orphanet:44200]
Contracture [Orphanet:44200]
Spasm [Orphanet:44200]
Quality:
Cross references:
Orphanet:44200 "Contractures/cramps/trismus/tetania/claudication/opisthotonos" [Orphanet:44200]
OMIM: "Opisthotonos" [OMIM:Opisthotonos]
OMIM: "Opisthotonus" [OMIM:Opisthotonus]
OMIM: "Opisthotonos (type II)" [OMIM:Opisthotonos (type II)]
UMLS:C0151818 "OPISTHOTONOS" [HPO:0002179]
UMLS:C0151818 "Opisthotonus" [Orphanet:44200]
UMLS:C0009917 "Contracture" [Orphanet:44200]
UMLS:C0037763 "Spasm" [Orphanet:44200]
Is a (Direct Parents):
Orphanet Muscle anomalies
MedDRA Dystonias
Orphanet Trismus
HPO         Spasticity
Is a (Whole tree): HPO:
All(HPO:0000001)
    Phenotypic abnormality(HPO:0000118)
       Abnormality of the nervous system(HPO:0000707)
          Abnormality of nervous system physiology(HPO:0012638)
             Abnormality of central motor function(HPO:0011442)
                Abnormal pyramidal signs(HPO:0007256)
                   Hypertonia(HPO:0001276)
                      Spasticity(HPO:0001257)
                         Opisthotonus(HPO:0002179)
MedDRA:
Nervous system disorders(MedDRA:10029205)
    Abnormality of movement(HPO:0100022)
       Dystonias(MedDRA:10013985)
          Opisthotonus(HPO:0002179)
Database Frequency: 35 / 7739
Resource:

All diseases associated with this symptom:

3-@METHYLCROTONYL-CoA CARBOXYLASE 1 DEFICIENCY (OMIM:210200)
ALG11-CDG (Orphanet:280071)
Acid phosphatase deficiency (Orphanet:35121)
Adenylosuccinate lyase deficiency (Orphanet:46)
Arnold-Chiari malformation type II (Orphanet:1136)
Buschke-Ollendorff syndrome (Orphanet:1306)
COLD-INDUCED SWEATING SYNDROME 1 (OMIM:272430)
Canavan disease (Orphanet:141)
Cold-induced sweating syndrome (Orphanet:157820)
Combined oxidative phosphorylation defect type 4 (Orphanet:254925)
D-glyceric aciduria (Orphanet:941)
Fetal Gaucher disease (Orphanet:85212)
GTP cyclohydrolase I deficiency (Orphanet:2102)
Gaucher disease type 2 (Orphanet:77260)
Gaucher disease type 3 (Orphanet:77261)
Glutaryl-CoA dehydrogenase deficiency (Orphanet:25)
Hepatoencephalopathy due to combined oxidative phosphorylation deficiency type 1 (Orphanet:137681)
Isolated 3-methylcrotonyl-CoA carboxylase deficiency (Orphanet:6)
LESCH-NYHAN SYNDROME (OMIM:300322)
Leigh syndrome (Orphanet:506)
Lesch-Nyhan syndrome (Orphanet:510)
MELAS (Orphanet:550)
Mohr-Tranebjaerg syndrome (Orphanet:52368)
Nephronophthisis 12 (OMIM:613820)
PONTOCEREBELLAR HYPOPLASIA, TYPE 2A (OMIM:277470)
PONTOCEREBELLAR HYPOPLASIA, TYPE 2B (OMIM:612389)
PONTOCEREBELLAR HYPOPLASIA, TYPE 2E (OMIM:615851)
Pontocerebellar hypoplasia type 2 (Orphanet:2524)
Pontocerebellar hypoplasia, type 9 (OMIM:615809)
Recessive hereditary methemoglobinemia type 1 (Orphanet:139373)
Recessive hereditary methemoglobinemia type 2 (Orphanet:139380)
Schinzel-Giedion syndrome (Orphanet:798)
Stiff person syndrome (Orphanet:3198)
Sulfite oxidase deficiency due to molybdenum cofactor deficiency type A (Orphanet:308386)
Sulfite oxidase deficiency due to molybdenum cofactor deficiency type B (Orphanet:308393)