ICD-10: E71.528

syndromic X-linked intellectual disability acrorenal syndrome Stormorken syndrome Vici syndrome chromosomal deletion syndrome stromal dystrophy MEDNIK syndrome EAST syndrome Schimke immuno-osseous dysplasia Kufor-Rakeb syndrome Holzgreve-Wagner-Rehder Syndrome 3MC syndrome 2 Yunis-Varon syndrome alpha-methylacyl-CoA racemase deficiency hypomyelinating leukodystrophy hypomyelinating leukodystrophy 10 hypomyelinating leukodystrophy 13 hypomyelinating leukodystrophy 12 syndromic X-linked intellectual disability Lubs type syndromic X-linked intellectual disability 5 Prieto syndrome syndromic X-linked intellectual disability Siderius type Wilson-Turner syndrome Miles-Carpenter syndrome syndromic X-linked intellectual disability Abidi type Christianson syndrome Griscelli syndrome type 1 Griscelli syndrome type 2 Griscelli syndrome type 3 Pierson syndrome obsolete genetic disorder Danon disease Alstrom syndrome Gamstorp-Wohlfart syndrome obsolete Majewski syndrome ABCD syndrome ADULT syndrome Bamforth-Lazarus syndrome bestrophinopathy Bjornstad syndrome Borjeson-Forssman-Lehmann syndrome Bowen-Conradi syndrome Brody myopathy Dent disease variable age at onset electroclinical syndrome AGAT deficiency ornithine translocase deficiency PHGDH deficiency PSAT deficiency X-linked monogenic disease obsolete CLN3 disease adenylosuccinase lyase deficiency mitochondrial complex V (ATP synthase) deficiency nuclear type 1 Ogden syndrome guanidinoacetate methyltransferase deficiency Kahrizi syndrome pyrimidine metabolic disorder Perrault syndrome non-syndromic intellectual disability X-linked hereditary ataxia janus kinase-3 deficiency CD45 deficiency Pearson syndrome Kennedy's disease Baraitser-Winter syndrome omodysplasia