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| Term | ichthyosis vulgaris | ID (Ontology) | DOID:1702 (Human Disease) |
| Definition | An ichthyosis that has_material_basis_in heterozygous mutation in the filaggrin gene (FLG) on chromosome 1q21 and is characterized by dead skin cells accumulate in thick, dry scales on your skin's surface. | ||
| Also Known As | "Dominant congenital ichthyosiform erythroderma" | ||
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Full annotation statements including this term (annotations to child terms are NOT included), and relevant FlyBase records
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autosomal genetic disease |__autosomal dominant disease__ skin disease | |__ichthyosis__________________| ichthyosis vulgaris |
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| Is a |
autosomal dominant disease ichthyosis |
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External Crossreferences & Linkouts
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GARD:6752 ICD10CM:Q80.0 MESH:D016112 MIM:146700 NCI:C84778 SNOMEDCT_US_2023_03_01:205551004 UMLS_CUI:C0079584 |
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