Disease: SPASTIC PARAPLEGIA 61, AUTOSOMAL RECESSIVE ×
Source: ALL
Disease Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
CUI: C3810294
Disease: SPASTIC PARAPLEGIA 61, AUTOSOMAL RECESSIVE
SPASTIC PARAPLEGIA 61, AUTOSOMAL RECESSIVE 		0.700 Biomarker disease GENOMICS_ENGLAND ARL6IP1 mutation causes congenital insensitivity to pain, acromutilation and spastic paraplegia. 28471035 2018
CUI: C3810294
Disease: SPASTIC PARAPLEGIA 61, AUTOSOMAL RECESSIVE
SPASTIC PARAPLEGIA 61, AUTOSOMAL RECESSIVE 		0.700 Biomarker disease GENOMICS_ENGLAND Exome sequencing links corticospinal motor neuron disease to common neurodegenerative disorders. 24482476 2014
CUI: C3810294
Disease: SPASTIC PARAPLEGIA 61, AUTOSOMAL RECESSIVE
SPASTIC PARAPLEGIA 61, AUTOSOMAL RECESSIVE 		0.700 GermlineCausalMutation disease ORPHANET Exome sequencing links corticospinal motor neuron disease to common neurodegenerative disorders. 24482476 2014
CUI: C3810294
Disease: SPASTIC PARAPLEGIA 61, AUTOSOMAL RECESSIVE
SPASTIC PARAPLEGIA 61, AUTOSOMAL RECESSIVE 		0.700 CausalMutation disease CLINVAR
CUI: C3810294
Disease: SPASTIC PARAPLEGIA 61, AUTOSOMAL RECESSIVE
SPASTIC PARAPLEGIA 61, AUTOSOMAL RECESSIVE 		0.700 Biomarker disease CTD_human