Spastic tetraparesis
Symptom Information:
Symptom ID: | HPO:0001285 | ||||
Synonyms: |
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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) Spastic tetraparesis(HPO:0001285) MedDRA: |
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Database Frequency: | 29 / 7739 | ||||
Resource: |
All diseases associated with this symptom:
AICARDI-GOUTIERES SYNDROME 7 | (OMIM:615846) |
ALZHEIMER DISEASE 3 | (OMIM:607822) |
AMYOTROPHIC LATERAL SCLEROSIS 2, JUVENILE | (OMIM:205100) |
Atypical Gaucher disease due to saposin C deficiency | (Orphanet:309252) |
Autosomal dominant spastic paraplegia type 31 | (Orphanet:101011) |
Autosomal recessive spastic paraplegia type 15 | (Orphanet:100996) |
Autosomal recessive spastic paraplegia type 35 | (Orphanet:171629) |
Beta-mannosidosis | (Orphanet:118) |
EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 7 | (OMIM:613720) |
Glutathione synthetase deficiency with 5-oxoprolinuria | (Orphanet:289846) |
Juvenile amyotrophic lateral sclerosis | (Orphanet:300605) |
Juvenile primary lateral sclerosis | (Orphanet:247604) |
KEPPEN-LUBINSKY SYNDROME | (OMIM:614098) |
L-2-hydroxyglutaric aciduria | (Orphanet:79314) |
LEUKOENCEPHALOPATHY, ARTHRITIS, COLITIS, AND HYPOGAMMAGLOBULINEMA | (OMIM:608809) |
Leukoencephalopathy - thalamus and brainstem anomalies - high lactate | (Orphanet:314051) |
Lissencephaly due to LIS1 mutation | (Orphanet:95232) |
METACHROMATIC LEUKODYSTROPHY DUE TO SAPOSIN B DEFICIENCY | (OMIM:249900) |
MICROCEPHALY 2, PRIMARY, AUTOSOMAL RECESSIVE, WITH OR WITHOUT CORTICALMALFORMATIONS | (OMIM:604317) |
MITOCHONDRIAL COMPLEX III DEFICIENCY, NUCLEAR TYPE 8 | (OMIM:615838) |
MULTIPLE EXOSTOSES WITH SPASTIC TETRAPARESIS | (OMIM:158345) |
Microcephaly-capillary malformation syndrome | (Orphanet:294016) |
Neurodegeneration with brain iron accumulation due to C19orf12 mutation | (Orphanet:289560) |
Ornithine transcarbamylase deficiency | (Orphanet:664) |
PONTOCEREBELLAR HYPOPLASIA, TYPE 1C | (OMIM:616081) |
Polyarteritis nodosa, childhood-onset | (OMIM:615688) |
Primary lateral sclerosis | (Orphanet:35689) |
Pyruvate dehydrogenase lipoic acid synthetase deficiency | (OMIM:614462) |
Sulfite oxidase deficiency due to molybdenum cofactor deficiency type A | (Orphanet:308386) |