Incoming and outgoing links Ichthyosis (overview)
Back to articleIncoming links
- Acanthosis
- Acitretin
- Acrodermatitis enteropathica
- ALOXE3 Gene
- Anhidrotic ectodermal dysplasia
- Brine bath
- Chondrodysplasia calcificans congenita
- Collodion baby
- Comel-netherton syndrome
- CYP4F22 Gene
- CYP4F22-Related Autosomal Recessive Congenital Ichthyosis
- Diogenes symptom complex
- Down syndrome
- Dystrophia myotonica
- Epidermolytic ichthyosis
- Erythrokeratodermia progressive, type burns
- Gluten-Related Dermatological Disorders
- Harlequin-ichthyosis
- Hypohidrosis
- Ichthyosis congenita
- Ichthyosis hand, or foot
- Ichthyosis hystrix
- Ichthyosis lamellosa and congenital (with preserved transglutaminase activity)
- Ichthyosis, paraneoplastic
- Ichthyosis simplex
- Ichthyosis, therapy
- Keratin
- Keratosis palmoplantaris with mutations in connexin 26
- KRT1 Gene
- Multiple sulphatase deficiency
- NIPAL4 Gene
- Oligohidrosis
- Onychogrypose
- Paraffins
- Pibi(d)s syndrome
- Pseudoichthyoses
- Refsum syndrome
- Rehabilitation, dermatological
- Salicylic acid
- Sebostasis
- Sjögren-larsson syndrome
- STIM1 Gene
- Superficial epidermolytic ichthyosis
Outgoing links
- ABHD5 Gene
- ALDH3A2 Gene
- Anular epidermolytic ichthyosis
- AP1S1 Gene
- ARKID syndrome
- Arthrogryposis-renal dysfunctional cholestasis
- Atrichia congenita with horny cysts
- CEDNIK syndrome
- Child syndrome
- Chondrodysplasia calcificans congenita
- CLDN1 Gene
- Comel-netherton syndrome
- Congenital reticular ichthyosiform erythroderma
- Dorfman-chanarin syndrome
- DSG1 Gene
- DSP Gene
- EBP Gene
- ELOVLA Gene
- Epidermolytic ichthyosis
- ERCC2 Gene
- Erythrokeratoderma (overview)
- GBA-gene
- GJB2 Gene
- Harlequin-ichthyosis
- Ichthyosis acquisita (pseudoichthyosis)
- Ichthyosis curth-macklin
- Ichthyosis follicularis with alopecia and photophobia
- Ichthyosis-hypotrichosis syndrome
- Ichthyosis-prematurity syndrome
- Ichthyosis, spastic quadriplegia, and mental retardation
- Ichthyosis, therapy
- Ichthyosis vulgaris
- Ichthyosis x-linked recessive
- Keratosis linearis-ichthyosis congenita-keratoderma with mutations in pomp
- Keratosis palmoplantaris with mutations in connexin 26
- Loricrin keratoderm
- MBTPS2 Gene
- MEDNIK syndrome
- MEND syndrome
- Multiple sulphatase deficiency
- Neonatal-ithyosis-sclerosing-cholangitis-syndrome
- Netherton syndrome
- Neuronopathic Gaucher disease
- Olmsted syndrome
- Palmoplantar keratoses (overview)
- Peeling skin syndrome
- PEX7 Gene
- PHYH Gene
- Refsum syndrome
- Severe dermatitis-multiple allergies-metabolic loss syndrome
- Sjögren-larsson syndrome
- SLC27A4 Gene
- SNAP29 Gene
- SPINK5 gene
- ST14 Gene
- STS Gene
- Superficial epidermolytic ichthyosis
- Trichothiodystrophy
- VPS33B Gene