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9 Result(s)

ORPHA:388   (Disorder)   Hirschsprung disease

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Keyword(s) : Zuelzer-Wilson syndrome

ORPHA:209919   (Disorder)   Idiopathic copper-associated cirrhosis

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Synonym(s) : Non-Wilsonian hepatic copper toxicosis of infancy and childhood

ORPHA:2152   (Disorder)   Mowat-Wilson syndrome

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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:905   (Disorder)   Wilson disease

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ORPHA:3459   (Disorder)   Wilson-Turner syndrome

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ORPHA:85290   (Disorder)   X-linked intellectual disability, Wilson type

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Keyword(s) : Mental retardation, X-linked, Wilson type