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#615516 - INTELLECTUAL DEVELOPMENTAL DISORDER, AUTOSOMAL RECESSIVE 38; MRT38
Cytogenetic locations: 616605
Gene summaries Genetic tests Medical literature
*605837 - HECT DOMAIN AND RCC1-LIKE DOMAIN 2; HERC2
Cytogenetic locations: mutation
#227220 - SKIN/HAIR/EYE PIGMENTATION, VARIATION IN, 1; SHEP1
Cytogenetic locations: 1p36, 1p36
#176270 - PRADER-WILLI SYNDROME; PWS
PRADER-WILLI SYNDROME CHROMOSOME REGION, INCLUDED; PWCR, INCLUDED
Cytogenetic locations: 12248305
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