Disease

hereditary spastic paraplegia 72A

Name: hereditary spastic paraplegia 72A
Creator: Alliance of Genome Resources
License: CC BY 4.0
Keywords: disease DOID:0110817 hereditary spastic paraplegia 72A A hereditary spastic paraplegia that has_material_basis_in a heterozygous mutation in the REEP2 gene on chromosome 5q31.2. SPG72 autosomal spastic paraplegia type 72

Definition

A hereditary spastic paraplegia that has_material_basis_in a heterozygous mutation in the REEP2 gene on chromosome 5q31.2.

Synonyms

autosomal spastic paraplegia type 72
SPG72

Cross References

ICD10CM:G11.4
MIM:615625

Parent Terms

autosomal dominant disease
autosomal recessive disease

Child Terms

None

Sources of Associations

RGD
MGI
ZFIN
FB
WB
SGD

Associated Genes

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Associated Alleles

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Associated Models

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