Opisthotonus
Symptom Information:
Symptom ID: | HPO:0002179 | |||||||||||||||||||||||
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 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) |
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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) |