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ORPHA:209919 (Disorder) Idiopathic copper-associated cirrhosis
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Synonym(s) : Non-Wilsonian hepatic copper toxicosis of infancy and childhood
ORPHA:261552 (Subtype of disorder) Mowat-Wilson syndrome due to a ZEB2 point mutation
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ORPHA:261537 (Subtype of disorder) Mowat-Wilson syndrome due to monosomy 2q22
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Synonym(s) : Mowat-Wilson syndrome due to del(2)q(22) ; Mowat-Wilson syndrome due to 2q22 microdeletion
ORPHA:85290 (Disorder) X-linked intellectual disability, Wilson type
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Keyword(s) : Mental retardation, X-linked, Wilson type