autosomal recessive congenital ichthyosis 8

Summary
Synonym
  • ARCI8
  • lamellar ichthyosis 4
  • late-onset lamellar ichthyosis
Definition
An autosomal recessive congenital ichthyosis characterized by diffuse lamellar ichthyosis, slight facial erythema, hyperkeratosis, orthokeratosis, hypergranulosis, and acanthosis that has_material_basis_in homozygous mutation in the LIPN gene on chromosome 10q23.
Super Class
autosomal recessive congenital ichthyosis
Disease Ontology
DOID:0060717
Mondo Disease Ontology
OMIM
Related Genes
Displaying 1 entry
Gene ID Gene Symbol Description Source
643418 LIPN lipase family member N
Displaying 1 entry
Gene ID Gene Symbol Description Source
70166 Lipn lipase, family member N
Displaying all 2 entries
Gene ID Gene Symbol Description Source
41643 Lip3 Lipase 3
43973 Lip1 Lipase 1
Displaying all 5 entries
Gene ID Gene Symbol Description Source
178563 lipl-5 Lipase lipl-5
178572 lipl-3 Lipase lipl-3
179046 lipl-4 Lipase lipl-4
179771 lipl-1 Lipase lipl-1
185840 lipl-2 Lipase
The Human Phenotype Ontology
Displaying entries 1 - 10 of 24 in total
HPO ID HPO Term
HP:0000989 Pruritus
HP:0011039 Abnormal helix morphology
HP:0000389 Chronic otitis media
HP:0100806 Sepsis
HP:0002205 Recurrent respiratory infections
HP:0000164 Abnormality of the dentition
HP:0008064 Ichthyosis
HP:0000958 Dry skin
HP:0100679 Lack of skin elasticity
HP:0001597 Abnormality of the nail
Displaying all 3 entries
Gene ID Gene Symbol Description
242 ALOX12B arachidonate 12-lipoxygenase, 12R type
643418 LIPN lipase family member N
6820 SULT2B1 sulfotransferase family 2B member 1

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Last updated: December 9, 2024