inherited ichthyosis
MONDO:0015947Mondo
Findings
No curated finding names inherited ichthyosis yet. Everything below is reference data from Mondo, HPO and GenCC, not evidence about what affects it.
Definition
Mendelian disorders of cornification affecting all or most of integument characterized by hyperkeratosis and/or scaling, caused by an inherited modification of the individual's genome.
Definition from the Mondo Disease Ontology (MONDO:0015947), read 2026-09-29. CC BY 4.0.
Where it sits
- A kind of
- Narrower terms (13)
- autosomal recessive congenital ichthyosis
- congenital cataract-ichthyosis syndrome
- ichthyosis hystrix
- ichthyosis linearis circumflexa
- ichthyosis vulgaris
- ichthyosis with erythrokeratoderma
- ichthyosis-oral and digital anomalies syndrome
- IFAP syndrome
- keratinopathic ichthyosis
- neonatal ichthyosis-sclerosing cholangitis syndrome
- Netherton syndrome
- peeling skin syndrome
- recessive X-linked ichthyosis
Other names
4 names
Resolves to: inherited ichthyosis
- Also called
- congenital ichthyosis of skingenetic ichthyosishereditary ichthyosis (disease)inherited genetic ichthyosis