Statements (26)
| Predicate | Object |
|---|---|
| gptkbp:instanceOf |
gptkb:skin
genetic disorder |
| gptkbp:affects |
gptkb:skin
|
| gptkbp:causedBy |
genetic disorder
|
| gptkbp:complication |
secondary infections
eye problems heat intolerance |
| gptkbp:containsGene |
CYP4F22
ABCA12 ALOX12B NIPAL4 TGM1 |
| gptkbp:frequency |
rare
|
| https://www.w3.org/2000/01/rdf-schema#label |
lamellar ichthyosis
|
| gptkbp:inheritance |
autosomal recessive
|
| gptkbp:onset |
at birth
|
| gptkbp:symptom |
scaly skin
dry skin thickened skin |
| gptkbp:synonym |
congenital ichthyosis
nonbullous congenital ichthyosiform erythroderma |
| gptkbp:treatment |
retinoids
moisturizers keratolytic agents |
| gptkbp:bfsParent |
gptkb:X-linked_ichthyosis
|
| gptkbp:bfsLayer |
7
|