(Q28024531)
English
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
Statements
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Identifiers
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