Names of Genes

Gene Chromosome Location Syndrome Category
WAC10p12.1Desanto-Shinawi syndromeAutism spectrum
WARBM420p13WARBURG MICRO SYNDROME 4Autism spectrum
WASHC58q24.13Spastic paraplegia type 8Copper metabolism defects
WDFY34q21.23Autism 18 (AUTS18)Autism spectrum
WDR349q34.11Short-rib thoracic dysplasia 13Cleft lip / cleft palate
WDR4523p11.23Beta-propeller protein-associated neurodegenerationAtaxia spectrum
WDR4523p11.23Rett SyndromeAutism spectrum
WDR4523p11.23beta-propeller protein-associated neurodegenerationEpilepsy and seizures
WDR607q36.3Short-rib thoracic dysplasia 13Cleft lip / cleft palate
WDR6219q13.12Autosomal recessive primary microcephalyMicrocephaly
WDR8117p13.3Cerebellar ataxia mental retardation and dysequilibrium syndrome type 02Ataxia spectrum
WDSTS11q23.3Wiedemann-Steiner syndromeAutism spectrum
WFS14p16.1Wolfram syndrome - diabetes mellitusDiabetes
WFS14p16.1Wolfram syndromeAtaxia spectrum
WFSL4p16.1WOLFRAM-LIKE SYNDROME AUTOSOMAL DOMINANTAutism spectrum
WHSC14p16.3Wolf-Hirschhorn syndromeCleft lip / cleft palate
WHSUS1q21.3WHITE-SUTTON SYNDROMEAutism spectrum
WITKOS15q24.2Witteveen-kolk syndromeAutism spectrum
WNT27q31.2 WINGLESS-TYPE MMTV INTEGRATION SITE FAMILY MEMBER 2Autism spectrum
WNT41p36.12Cerebral palsy - unassignedCerebral palsy
WNT7A3p25.1ALSALS - amyotrophic lateral sclerosis
WRN8p12Werner syndromeCataracts
WRN8p12Type 2 DiabetesDiabetes
WRN8p12Thyroid disordersHypothyroidism
WS2E22q13.1WAARDENBURG SYNDROME TYPE 2EAutism spectrum
WT111p13WAGR SyndromeAutism spectrum
WWOX16q23.1-2Spinocerebellar ataxia autosomal recessive type 12Ataxia spectrum


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