hereditary spastic paraplegia 25 https://github.com/monarch-initiative/mondo/issues/6752 https://github.com/monarch-initiative/mondo/issues/6878 https://www.malacards.org/card/spastic_paraplegia_25_autosomal_recessive spinal disc herniation with autosomal recessive spastic paraplegia autosomal recessive spastic paraplegia-disc herniation syndrome Orphanet:101005 GARD:0009582 hereditary spastic paraplegia type 25 SPG25 MESH:C536861 MONDO:0011992 Autosomal recessive spastic paraplegia type 25 (SPG25) is a rare, complex type of hereditary spastic paraplegia characterized by adult-onset spastic paraplegia associated with spinal pain that radiates to the upper or lower limbs and is related to disk herniation (with minor spondylosis), as well as mild sensorimotor neuropathy. The SPG25 phenotype has been mapped to a locus on chromosome 6q23-q24.1. SCTID:732933009 spastic paraplegia 25 spastic paraplegia 25, autosomal recessive OMIM:608220 autosomal recessive spastic paraplegia type 25 DOID:0110776 spinal disk herniation with autosomal recessive spastic paraplegia UMLS:C2936860 MEDGEN:424835 complex hereditary spastic paraplegia