WormBase Tree Display for DO_term: DOID:0110843
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| DOID:0110843 | Name | xeroderma pigmentosum group A | |||
|---|---|---|---|---|---|
| Status | Valid | ||||
| Definition | A xeroderma pigmentosum characterized by involvement of the central and peripheral nervous systems in addition to cutaneous lesions that has_material_basis_in caused by homozygous or compound heterozygous mutation in the XPA gene on chromosome 9q22. | ||||
| Synonym | Exact | XP group A | |||
| XP1 | |||||
| XPA | |||||
| xeroderma pigmentosum 1 | |||||
| xeroderma pigmentosum complementation group A | |||||
| Parent | Is_a | DOID:0050427 | |||
| DB_info | Database | OMIM | disease | 278700 | |
| Attribute_of | Gene_by_orthology | WBGene00006963 |
