Overview
Mental retardation, X-linked (NGS panel for 89 genes)
This is a clinical test intended for HelpPurposes or indications for the test. Lab-provided.: Diagnosis
49 conditions tested. Click Indication tab for more information.
- Mental retardation 63, X-linked (MRX63)
- Aarskog syndrome (AAS)
- Christianson syndrome (MRXSCH)
- Corpus callosum, agenesis of, with mental retardation, ocular coloboma, and micrognathia
- Creatine deficiency, X-linked (CCDS1)
- Deficiency of glycerol kinase (GKD)
- Duchenne muscular dystrophy (DMD)
- Dyskeratosis congenita X-linked (DKCX)
- Early infantile epileptic encephalopathy 2 (EIEE2)
- Early infantile epileptic encephalopathy 8 (EIEE8)
- FRAXE
- Fragile X syndrome (FXS)
- Lissencephaly, X-linked (LISX1)
- MECP2 duplication syndrome (MRXSL)
- Mental retardation 21, X-linked (MRX21)
- Mental retardation 3, X-linked (MRX3)
- Mental retardation 30, X-linked (MRX30)
- Mental retardation 46, X-linked (MRX46)
- Mental retardation 58, X-linked (MRX58)
- Mental retardation 9, X-linked (MRX9)
- Mental retardation X-linked with cerebellar hypoplasia and distinctive facial appearance
- Mental retardation and microcephaly with pontine and cerebellar hypoplasia (MICPCH)
- Mental retardation, X-linked 19 (MRX19)
- Mental retardation, X-linked 45 (MRX45)
- Mental retardation, X-linked 72 (MRX72)
- Mental retardation, X-linked 93 (MRX93)
- Mental retardation, X-linked 96 (MRX96)
- Mental retardation, X-linked 98 (MRX98)
- Mental retardation, X-linked, syndromic 10 (MRXS10)
- Mental retardation, X-linked, syndromic 32 (MRXS32)
- Mental retardation, X-linked, syndromic, Hedera type (MRXSH)
- Mental retardation, X-linked, syndromic, Turner type (MRXST), lab preferred: Mental retardation, X-linked, syndromic, turner type
- Mental retardation, X-linked, syndromic, wu type (MRXSW)
- Mental retardation, syndromic 14, X-linked (MRXS14)
- Mental retardation, syndromic, Claes-Jensen type, X-linked (MRXSCJ)
- Mental retardation, with or without seizures, ARX-related, X-linked (MRXARX)
- Mental retardation-hypotonic facies syndrome X-linked, 1 (MRXHF1)
- Pettigrew syndrome (PGS), lab preferred: Mental retardation X-linked syndromic 5
- Renpenning syndrome 1 (RENS1)
- Rolandic epilepsy with mental retardation and speech dyspraxia, X-linked (RESDX)
- Siderius X-linked mental retardation syndrome (MRXSSD)
- Snyder Robinson syndrome (MRXSSR)
- Stocco dos Santos syndrome (SDSX)
- Syndromic X-linked mental retardation, Cabezas type (MRXSC)
- Syndromic mental retardation, Nascimento type, X-linked (MRXSN)
- Wilson-Turner X-linked mental retardation syndrome (WTS)
- X-Linked Mental Retardation 41 (MRX41)
- X-Linked mental retardation 90 (MRX90)
- ZNF711-Related X-linked Mental Retardation (MRX97)
- Molecular Genetics
- CSequence analysis of the entire coding region
- Next-Generation (NGS)/Massively parallel sequencing (MPS)
Summary of what is tested
89 genes and variants. Click Methodology tab for more information.
Genes
Not provided
Not provided
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