Spastic tetraparesis

Symptom Information:

Symptom ID: HPO:0001285
Synonyms:
Spastic quadriparesis [HPO:0001285]
Spastic quadriparesis [OMIM:Spastic quadriparesis]
Spastic tetraparesis [OMIM:Spastic tetraparesis]
Spastic tetraparesis (in severe cases) [OMIM:Spastic tetraparesis (in severe cases)]
Quality:
Cross references:
OMIM: "Spastic quadriparesis" [OMIM:Spastic quadriparesis]
OMIM: "Spastic tetraparesis" [OMIM:Spastic tetraparesis]
OMIM: "Spastic tetraparesis (in severe cases)" [OMIM:Spastic tetraparesis (in severe cases)]
Is a (Direct Parents):
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)
                         Spastic tetraparesis(HPO:0001285)
MedDRA:
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)