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Disease association ontology term - MONDO:0019064 - hereditary spastic paraplegia

Term summary

ID
MONDO:0019064
Name
hereditary spastic paraplegia
Ontology or CV name
Disease association
Definition
Hereditary spastic paraplegias (HSP) comprise a genetically and clinically heterogeneous group of neurodegenerative disorders characterized by progressive spasticity and hyperreflexia of the lower limbs.

Parents

Annotation

Disease association

MONDO:0014702 - autosomal recessive complex spastic paraplegia type 9B

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MONDO:0018422 - autosomal recessive spastic paraplegia type 70

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MONDO:0014975 - autosomal recessive spastic paraplegia type 78

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MONDO:0014567 - glutamate pyruvate transaminase 2 deficiency

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MONDO:0009748 - hereditary sensory and autonomic neuropathy with spastic paraplegia

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MONDO:0011408 - hereditary spastic paraplegia 10

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MONDO:0011489 - hereditary spastic paraplegia 12

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MONDO:0011532 - hereditary spastic paraplegia 13

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MONDO:0010043 - hereditary spastic paraplegia 17

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MONDO:0012256 - hereditary spastic paraplegia 28

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MONDO:0012453 - hereditary spastic paraplegia 31

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MONDO:0012866 - hereditary spastic paraplegia 35

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MONDO:0012787 - hereditary spastic paraplegia 39

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MONDO:0008438 - hereditary spastic paraplegia 4

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MONDO:0012928 - hereditary spastic paraplegia 42

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MONDO:0014018 - hereditary spastic paraplegia 54

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MONDO:0014020 - hereditary spastic paraplegia 55

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MONDO:0014305 - hereditary spastic paraplegia 63

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MONDO:0014282 - hereditary spastic paraplegia 72

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MONDO:0014644 - hereditary spastic paraplegia 74

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MONDO:0014882 - hereditary spastic paraplegia 77

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MONDO:0011006 - hereditary spastic paraplegia 9A

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MONDO:0012651 - spastic ataxia 2

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MONDO:0700307 - spastic paraplegia 30A, autosomal dominant

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MONDO:0971149 - spastic paraplegia 30B, autosomal recessive

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MONDO:0957958 - spastic paraplegia 72b, autosomal recessive

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MONDO:0032906 - spastic paraplegia 82, autosomal recessive

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MONDO:0030482 - spastic paraplegia 84, autosomal recessive

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MONDO:0030512 - spastic paraplegia 85, autosomal recessive

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MONDO:0031019 - spastic paraplegia 87, autosomal recessive

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MONDO:0957308 - spastic paraplegia 90A, autosomal dominant

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MONDO:0957309 - spastic paraplegia 90B, autosomal recessive

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MONDO:0975796 - spastic paraplegia 93, autosomal recessive

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