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| Term | keratosis palmoplantaris striata 1 | ID (Ontology) | DOID:0081108 (Human Disease) |
| Definition | A keratosis palmoplantaris striata that is characterized by hyperkeratotic lesions that are restricted to the pressure regions extending longitudinally in the length of each finger to the palm and that has_material_basis_in heterozygous mutation in the DSG1 gene on chromosome 18q12. | ||
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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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No relevant statements available
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autosomal genetic disease |__autosomal dominant disease________ palmoplantar keratosis | |__keratosis palmoplantaris striata__| keratosis palmoplantaris striata 1 |
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| Is a |
autosomal dominant disease keratosis palmoplantaris striata |
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External Crossreferences & Linkouts
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GARD:9172 MESH:C536162 MIM:148700 ORDO:369999 ORDO:370002 |
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