Genomics England
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Genes and Entities
ARL6IP1
ADP ribosylation factor like GTPase 6 interacting protein 1
OMIM:
607669
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Panel
Mode of inheritance
Details
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Childhood onset hereditary spastic paraplegia
R-numbers:
R61
Signed-off version 7.0
BIALLELIC, autosomal or pseudoautosomal
Phenotypes
Spastic paraplegia 61, autosomal recessive, OMIM:615685, hereditary spastic paraplegia 61, MONDO:0014304