Preferred Name |
piebaldism |
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Synonyms |
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Definitions |
An integumentary system disease characterized by congenital absence of melanocytes in areas of the skin and hair that has_material_basis_in heterozygous mutation in either KIT or SNAI2 on chromosome 4q12 or 8q11.21, respectively. |
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ID |
http://purl.obolibrary.org/obo/DOID_3263 |
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definition |
An integumentary system disease characterized by congenital absence of melanocytes in areas of the skin and hair that has_material_basis_in heterozygous mutation in either KIT or SNAI2 on chromosome 4q12 or 8q11.21, respectively. |
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imported from | ||
label |
piebaldism |
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prefixIRI |
DOID:3263 |
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prefLabel |
piebaldism |
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subClassOf |
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