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Human Disease
autosomal recessive congenital ichthyosis 7
- Term ID
- DOID:0060716
- Synonyms
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- ARCI7
- Definition
- An autosomal recessive congenital ichthyosis characterized by fine whitish scales, moderate to severe erythroderma, compact hyperkeratosis, hypergranulosis, acanthosis, and papillomatosis that has_material_basis_in variation in the chromosome region 12p11.2-q13.1. https://www.ncbi.nlm.nih.gov/pubmed/16117785
- References
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- ICD10CM:Q80.2
- MIM:615022
- Ontology
- Human Disease ( DOID:0060716 )
- is a type of
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Genes Involved
Zebrafish Models