Spastic tetraplegia
Symptom Information:
Symptom ID: | HPO:0002510 | ||||||
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) Spastic tetraplegia(HPO:0002510) MedDRA: |
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Database Frequency: | 54 / 7739 | ||||||
Resource: |
All diseases associated with this symptom:
3-methylglutaconic aciduria type 1 | (Orphanet:67046) |
3-phosphoglycerate dehydrogenase deficiency | (Orphanet:79351) |
ASPARAGINE SYNTHETASE DEFICIENCY | (OMIM:615574) |
Aldosterone-producing adenoma with seizures and neurological abnormalities | (Orphanet:369929) |
Allan-Herndon-Dudley syndrome | (Orphanet:59) |
Anophthalmia/microphthalmia - esophageal atresia | (Orphanet:77298) |
Autosomal recessive spastic paraplegia type 11 | (Orphanet:2822) |
Beta-mannosidosis | (Orphanet:118) |
CEREBRAL PALSY, SPASTIC QUADRIPLEGIC, 1 | (OMIM:603513) |
CEREBRAL PALSY, SPASTIC QUADRIPLEGIC, 2 | (OMIM:612900) |
CORTICAL DYSPLASIA, COMPLEX, WITH OTHER BRAIN MALFORMATIONS 2 | (OMIM:615282) |
CORTICAL DYSPLASIA, COMPLEX, WITH OTHER BRAIN MALFORMATIONS 3 | (OMIM:615411) |
CORTICAL DYSPLASIA, COMPLEX, WITH OTHER BRAIN MALFORMATIONS 4 | (OMIM:615412) |
Congenital ichthyosis - intellectual deficit - spastic quadriplegia | (Orphanet:352333) |
D-glyceric aciduria | (Orphanet:941) |
EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 11 | (OMIM:613721) |
EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 4 | (OMIM:612164) |
EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 5 | (OMIM:613477) |
Familial acute necrotizing encephalopathy | (Orphanet:88619) |
Fucosidosis | (Orphanet:349) |
GM1 gangliosidosis type 2 | (Orphanet:79256) |
Galloway-Mowat syndrome | (Orphanet:2065) |
Hypotonia with lactic acidemia and hyperammonemia | (Orphanet:137908) |
Hypotonia-speech impairment-severe cognitive delay syndrome | (Orphanet:371364) |
Infantile neuroaxonal dystrophy | (Orphanet:35069) |
Infantile-onset ascending hereditary spastic paralysis | (Orphanet:293168) |
Inherited congenital spastic tetraplegia | (Orphanet:210141) |
Leigh syndrome with leukodystrophy | (Orphanet:255241) |
Lissencephaly due to TUBA1A mutation | (Orphanet:171680) |
MENTAL RETARDATION, AUTOSOMAL DOMINANT 13 | (OMIM:614563) |
METACHROMATIC LEUKODYSTROPHY | (OMIM:250100) |
MICROCEPHALY WITH SPASTIC QUADRIPLEGIA | (OMIM:251280) |
MICROHYDRANENCEPHALY | (OMIM:605013) |
Micrencephaly - corpus callosum agenesis - abnormal genitalia | (Orphanet:2508) |
Mucolipidosis type 4 | (Orphanet:578) |
NEURODEGENERATION WITH BRAIN IRON ACCUMULATION 2A | (OMIM:256600) |
NEURODEGENERATION WITH BRAIN IRON ACCUMULATION 6 | (OMIM:615643) |
Neurologic Waardenburg-Shah syndrome | (Orphanet:163746) |
OPTICOCOCHLEODENTATE DEGENERATION | (OMIM:258700) |
PONTOCEREBELLAR HYPOPLASIA, TYPE 2D | (OMIM:613811) |
PONTOCEREBELLAR HYPOPLASIA, TYPE 2E | (OMIM:615851) |
Pyruvate dehydrogenase E1-alpha deficiency | (Orphanet:79243) |
Pyruvate dehydrogenase E3 deficiency | (Orphanet:2394) |
Pyruvate dehydrogenase E3-binding protein deficiency | (Orphanet:255182) |
Pyruvate dehydrogenase lipoic acid synthetase deficiency | (OMIM:614462) |
SPASTIC PARAPLEGIA 50, AUTOSOMAL RECESSIVE | (OMIM:612936) |
SPASTIC PARAPLEGIA 51, AUTOSOMAL RECESSIVE | (OMIM:613744) |
Severe intellectual deficit and progressive spastic paraplegia | (Orphanet:280763) |
Spastic tetraplegia - retinitis pigmentosa - intellectual deficit | (Orphanet:3011) |
Sulfite oxidase deficiency due to molybdenum cofactor deficiency type A | (Orphanet:308386) |
Sulfite oxidase deficiency due to molybdenum cofactor deficiency type B | (Orphanet:308393) |
WARBURG MICRO SYNDROME 3 | (OMIM:614222) |
WARBURG MICRO SYNDROME 4 | (OMIM:615663) |
X-linked intellectual disability-cardiomegaly-congestive heart failure syndrome | (Orphanet:324410) |