syndromic intellectual disability syndromic disease hereditary disease spastic tetraplegia-retinitis pigmentosa-intellectual disability syndrome https://github.com/monarch-initiative/mondo/issues/5588 https://github.com/monarch-initiative/mondo/issues/6744 https://github.com/monarch-initiative/mondo/issues/6750 https://github.com/monarch-initiative/mondo/issues/6752 https://github.com/monarch-initiative/mondo/issues/6877 https://github.com/monarch-initiative/mondo/issues/6878 https://www.malacards.org/card/spastic_quadriplegia_retinitis_pigmentosa_and_impaired_intellectual_development https://www.malacards.org/card/spastic_tetraplegia_retinitis_pigmentosa_intellectual_disability_syndrome MEDGEN:376519 MONDO:0010051 GARD:0004932 This term's classification was reviewed in the context of the Strategic Refinement project (2023) and was determined to be excluded from the 'metabolic disease' (MONDO:0005066) ontology branch (https://orcid.org/0000-0002-1780-5230) MESH:C564808 progressive quadriparesis, intellectual disability, retinitis pigmentosa and hearing loss Spastic tetraplegia-retinitis pigmentosa-intellectual disability syndrome is characterized by nonprogressive spastic paraplegia, retinitis pigmentosa, and intellectual deficit. It has been described in two brothers born to consanguineous parents. spastic quadriplegia-retinitis pigmentosa-intellectual disability syndrome spastic quadriplegia retinitis pigmentosa intellectual disability UMLS:C1849112 progressive quadriparesis, mental retardation, retinitis pigmentosa and hearing loss Orphanet:3011 spastic quadriplegia retinitis pigmentosa mental retardation OMIM:270950 spastic quadriplegia, retinitis pigmentosa, and mental retardation