MeSH Treeview
Query OMIM entry list
611252
SPG32
SPASTIC PARAPLEGIA 32, AUTOSOMAL RECESSIVE
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Genetic Phenomena
Consanguinity
Genetic Processes
Breeding
Inbreeding
Consanguinity
Genetic Structures
Chromosomes
Chromosomes, Mammalian
Chromosomes, Human
Chromosomes, Human, 13-15
Chromosomes, Human, Pair 14
Genetic Variation
Mutation
Genotype
Genetic Predisposition to Disease
Inheritance Patterns
Phenotype
Genetic Markers
Database Center for Life Science
