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Exfoliative ichthyosis
1 OMIM reference -
1 associated gene
22 connected diseases
No signs/symptoms info
Disease Type of connection
Keratosis palmoplantaris striata
Narcolepsy-cataplexy
Annular epidermolytic ichthyosis
Epidermolytic ichthyosis
Epidermolytic palmoplantar keratoderma
Familial isolated arrhythmogenic ventricular dysplasia, biventricular form
Familial isolated arrhythmogenic ventricular dysplasia, left dominant form
Familial isolated arrhythmogenic ventricular dysplasia, right dominant form
Ichthyosis hystrix of Curth-Macklin
Idiopathic pulmonary fibrosis
Keratoderma hereditarium mutilans with ichthyosis
Lethal acantholytic epidermolysis bullosa
Progressive symmetric erythrokeratodermia
Skin fragility-woolly hair-palmoplantar keratoderma syndrome
Woolly hair-palmoplantar keratoderma-dilated cardiomyopathy syndrome
Autosomal agammaglobulinemia
Cabezas syndrome
Cornelia de Lange syndrome
Giant cell glioblastoma
Gliosarcoma
Mosaic variegated aneuploidy syndrome
Precursor B-cell acute lymphoblastic leukemia
Synonym(s):
- Autosomal recessive exfoliative ichthyosis
- Ichthyosis exfoliativa
Classification (Orphanet):
- Rare genetic disease
- Rare skin disease
Classification (ICD10):
- Congenital malformations, deformations and chromosomal abnormalities -
Epidemiological data:
Class of prevalence: unknown
Average age onset: neonatal/infancy
Average age of death: -
Type of inheritance: autosomal recessive
External references:
1 OMIM reference -
No MeSH references
Gene symbol UniProt reference OMIM reference
CSTA P01040184600
No signs/symptoms info available.