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GTR Home > Conditions/Phenotypes > Hereditary spastic paraplegia 61

Hereditary spastic paraplegia 61

Synonyms
Spastic paraplegia 61, autosomal recessive
Modes of inheritance
Autosomal recessive inheritance (Orphanet)

Summary

Autosomal recessive spastic paraplegia-61 (SPG61) is a complicated, early-onset spastic paraplegia (summary by Chukhrova et al., 2019). [from OMIM]

Available tests

12 tests are in the database for this condition.

Check Related conditions for additional relevant tests.

Clinical tests (12 available)

Molecular Genetics Tests

Genes See tests for all associated and related genes

  • Also known as: AIP1, ARL6IP, ARMER, SPG61, ARL6IP1
    Summary: ADP ribosylation factor like GTPase 6 interacting protein 1

Clinical features

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Imported from Human Phenotype Ontology (HPO)

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