WormBase Tree Display for DO_term: DOID:0050467
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DOID:0050467 | Name | erythrokeratodermia variabilis | |
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Status | Valid | ||
Definition | A skin disease that is characterized by areas of sharply demarcated, brown hyperkeratosis and has_material_basis_in mutations in genes encoding for connexin channels proteins in the epidermis. | ||
Comment | OMIM mapping confirmed by DO. | ||
Synonym | Exact (2) | ||
Parent | Is_a (2) | ||
Child | Is (6) | ||
Attribute_of | Gene_by_orthology | WBGene00006875 |