WormBase Tree Display for DO_term: DOID:0050467
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| DOID:0050467 | Name | erythrokeratodermia variabilis | |
|---|---|---|---|
| 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 | Erythrokeratodermia Figurata Variabilis | |
| Greither Disease | |||
| Parent | Is_a | DOID:37 | |
| DOID:0050177 | |||
| Child | Is | DOID:0080248 | |
| DOID:0080249 | |||
| DOID:0080250 | |||
| DOID:0080251 | |||
| DOID:0080766 | |||
| DOID:0111195 | |||
| Attribute_of | Gene_by_orthology | WBGene00006875 |
