Preferred Label : spastic paraplegia 32 (autosomal recessive);
Obsolete resource : true;
Approved symbol HGNC : SPG32;
Alias symbols HGNC : SPG29;
Chromosome HGNC : 14q12-q21;
Locus type HGNC : phenotype;
Origin ID : HGNC:32314;
UMLS CUI : C1823103;
Automatic exact mappings (from CISMeF team)
Orphanet gene
Semantic type(s)