autosomal recessive congenital ichthyosis 5 ^{الإنجليزية} (Q5740177)

مرض يصيب الإنسان

اللغة	التسمية	الوصف	أسماء أخرى
العربية	لم تُضف التسمية	مرض يصيب الإنسان
الإنجليزية	autosomal recessive congenital ichthyosis 5	autosomal recessive congenital ichthyosis characterized by fine white or greyish-white scales, hyperkeratosis, moderate acanthosis, and moderate parakeratosis that has material basis in homozygous mutation in the CYP4F22 gene on chromosome 19p13	ARCI5 autosomal recessive congenital nonlamellar and nonerythrodermic ichthyosis Ichthyosis Congenita 3 autosomal recessive congenital ichthyosis type 5 NNCI Ichthyosis, Congenital, Autosomal Recessive type 5 Ichthyosis Congenita III LI3, FORMERLY Ichthyosis, Lamellar, 3, Formerly Ichthyosis, Nonlamellar and Nonerythrodermic, Congenital, Autosomal Recessive ICHTHYOSIS, CONGENITAL, AUTOSOMAL RECESSIVE 5; ARCI5 Ichthyosis, Lamellar, 3 Type 3 lamellar ichthyosis ICHTHYOSIS, CONGENITAL, AUTOSOMAL RECESSIVE 5 Lamellar ichthyosis, type 3 Ichthyosis lamellar 3

بيانات

Wikidata item ^{الإنجليزية}

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