Genomics England
GMS Panels
Panels
Genes and Entities
AMFR
autocrine motility factor receptor
OMIM:
603243
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Panel
Mode of inheritance
Details
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Childhood onset hereditary spastic paraplegia
R-numbers:
R61
Signed-off version 5.3
BIALLELIC, autosomal or pseudoautosomal
Phenotypes
Spastic paraplegia 89, autosomal recessive, OMIM:620379