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Disease association ontology term - MONDO:0015150 - complex hereditary spastic paraplegia

Term summary

ID
MONDO:0015150
Name
complex hereditary spastic paraplegia
Ontology or CV name
Disease association
Definition
A hereditary spastic paraplegia that is part of a larger syndrome.

Parents

Annotation

Disease association

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

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Genes:

MONDO:0018422 - autosomal recessive spastic paraplegia type 70

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Genes:

MONDO:0014975 - autosomal recessive spastic paraplegia type 78

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Genes:

MONDO:0014567 - glutamate pyruvate transaminase 2 deficiency

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Genes:

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

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Genes:

MONDO:0010043 - hereditary spastic paraplegia 17

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Genes:

MONDO:0012787 - hereditary spastic paraplegia 39

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Genes:

MONDO:0014018 - hereditary spastic paraplegia 54

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MONDO:0014020 - hereditary spastic paraplegia 55

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Genes:

MONDO:0014305 - hereditary spastic paraplegia 63

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Genes:

MONDO:0014644 - hereditary spastic paraplegia 74

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MONDO:0011006 - hereditary spastic paraplegia 9A

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Genes:

MONDO:0012651 - spastic ataxia 2

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Genes:

MONDO:0030482 - spastic paraplegia 84, autosomal recessive

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Genes:

MONDO:0030512 - spastic paraplegia 85, autosomal recessive

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