has material basis in germline mutation in WNK3 Prieto syndrome https://github.com/monarch-initiative/mondo/issues/4521 https://github.com/monarch-initiative/mondo/issues/5588 https://github.com/monarch-initiative/mondo/issues/9285 https://www.malacards.org/card/prieto_syndrome UMLS:C1839730 GARD:0004482 Orphanet:2958 Prieto-Badia-Mulas syndrome This syndrome is characterized by intellectual deficit associated with facial dysmorphism, patella luxation, and abnormal growth of the teeth. MRXS2 MESH:C535274 OMIM:309610 MONDO:0010667 Prieto X-linked mental retardation syndrome MEDGEN:374294 SCTID:719140001 X-linked intellectual disability-dysmorphism-cerebral atrophy syndrome PRS Prieto syndrome, X-linked recessive mental retardation, X-linked, with Dysmorphism and cerebral atrophy Prieto X-linked intellectual disability syndrome DOID:0060805 mental retardation, X-linked, syndromic 2 X-linked syndromic intellectual disability