160. Congenital ichthyosis Disease details / Clinical trials / Drug dev / DR info
Clinical trials : 42 / Drugs : 71 - (DrugBank : 21) / Drug target genes : 18 - Drug target pathways : 112
Previous names | - | ||
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Other names | - | ||
Disease group | Skin and connective tissue diseases | ||
Related info (in Japanese) | |||
Designated intractable diseases (in Japanese) | Overview, Diagnostic criteria, etc. (docx), Clinical research form (pdf) | ||
Specific pediatric chronic diseases, Japan (in Japanese) | 14-2-3. autosomal recessive congenital ichthyosis (excluding harlequin ichthyosis) | ||
14-2-5. Netherton syndrome | |||
14-2-7. Other congenital ichthyoses | |||
Subtypes | No. | Name | Specific pediatric chronic diseases, Japan (in Japanese) |
160-1. | Keratinopathic ichthyosis; | 14-2-2. keratinopathic ichthyosis (including epidermolytic ichthyosis and superficial epidermolytic ichthyos | |
160-2. | Epidermolytic ichthyosis; | 14-2-2. keratinopathic ichthyosis (including epidermolytic ichthyosis and superficial epidermolytic ichthyos | |
160-3. | Superficial epidermolytic ichthyosis; | 14-2-2. keratinopathic ichthyosis (including epidermolytic ichthyosis and superficial epidermolytic ichthyos | |
160-4. | Harlequin ichthyosis; | 14-2-4. harlequin ichthyosis | |
160-5. | Autosomal recessive congenital ichthyosis; | ||
160-6. | Congenital Ichthyosiform Erythroderma; | ||
160-7. | Foliate ichthyosis; | ||
160-8. | Ichthyosis syndrome; | ||
160-9. | Netherton syndrome; | 14-2-5. Netherton syndrome | |
160-10. | Sjogren-Larsson syndrome;Sjögren-Larsson syndrome; | 14-2-6. Sjögren-Larsson syndrome | |
160-11. | Keratitis-ichtyosis-deafness syndrome; | 14-2-7. Other congenital ichthyoses | |
160-12. | Dorfman-Chanarin syndrome; | 14-2-7. Other congenital ichthyoses | |
160-13. | Neutral lipid storage disease;NLSD; | ||
160-14. | Multiple sulfatase deficiency;Austin disease; | 8-6-94. Multiple sulfatase deficiency | |
160-15. | Recessive X-linked ichthyosis;RXLI;X-linked recessive ichthyosis; | ||
160-16. | Ichthyosis, brittle hair, impaired intelligence, decreased fertility and short stature;IBID; | ||
160-17. | Trichothiodystrophy; | ||
160-18. | Follicular ichthyosis; | ||
160-19. | Congenital hemidysplasia, ichthyosiform erythroderma or nevus, and limb defects syndrome;CHILD syndrome; | 14-2-7. Other congenital ichthyoses | |
160-20. | Conradi-Hunermann-Happle syndrome;Conradi-Hünermann-Happle syndrome;CHHS; |