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autosomal recessive congenital ichthyosis 5
Summary
- Synonym
-
- ARCI5
- autosomal recessive congenital nonlamellar and nonerythrodermic ichthyosis
- Definition
- An autosomal recessive congenital ichthyosis characterized by fine white or greyish-white scales, hyperkeratosis, moderate acanthosis, and moderate parakeratosis that has_material_basis_in homozygous mutation in the CYP4F22 gene on chromosome 19p13.
- Super Class
- autosomal recessive congenital ichthyosis
External Links
- Disease Ontology
- DOID:0060714
- Mondo Disease Ontology
- OMIM
Related Genes
| Gene ID | Gene Symbol | Description | Source |
|---|---|---|---|
| 224 | ALDH3A2 | aldehyde dehydrogenase 3 family member A2 | |
| 242 | ALOX12B | arachidonate 12-lipoxygenase, 12R type | |
| 412 | STS | steroid sulfatase | |
| 1555 | CYP2B6 | cytochrome P450 family 2 subfamily B member 6 | |
| 2629 | GBA1 | glucosylceramidase beta 1 | |
| 6820 | SULT2B1 | sulfotransferase family 2B member 1 | |
| 91949 | COG7 | component of oligomeric golgi complex 7 | |
| 204219 | CERS3 | ceramide synthase 3 |
Related Glycoprotein
| UniProt ID | Protein Name | Source |
|---|---|---|
| O75342 | Arachidonate 12-lipoxygenase, 12R-type | |
| P04062 | Lysosomal acid glucosylceramidase | |
| P08842 | Steryl-sulfatase | |
| P51648 | Aldehyde dehydrogenase family 3 member A2 | |
| P83436 | Conserved oligomeric Golgi complex subunit 7 |
- The Human Phenotype Ontology
| HPO ID | HPO Term |
|---|---|
| HP:0000083 | Renal insufficiency |
| HP:0000164 | Abnormality of the dentition |
| HP:0000232 | Everted lower lip vermilion |
| HP:0000389 | Chronic otitis media |
| HP:0000656 | Ectropion |
| HP:0000958 | Dry skin |
| HP:0000962 | Hyperkeratosis |
| HP:0000989 | Pruritus |
| HP:0001019 | Erythroderma |
| HP:0001597 | Abnormality of the nail |
