|
| General Information | |||
|---|---|---|---|
| Term | epidermodysplasia verruciformis | ID (Ontology) | DOID:13777 (Human Disease) |
| Definition | A primary immunodeficiency disease that results_in skin squamous cell carcinoma located_in skin, associated with a high risk of carcinoma. It is characterized by abnormal susceptibility to human papillomaviruses of the skin and has_symptom lesions on the body. | ||
| Comment | |||
| Links to External Ontologies | |||
| DO.org | |||
| Annotations | |||
| Records annotated with this term OR any of its CHILD TERMS | |||
Full annotation statements including this term (annotations to child terms are NOT included), and relevant FlyBase records
|
|||
|
No relevant statements available
|
|||
|
||||||
autosomal genetic disease |__autosomal recessive disease_______ immune system disease | |__primary immunodeficiency disease__| epidermodysplasia verruciformis |
| Spanning Tree View Settings | |||
|---|---|---|---|
| Parents/Children View Depth |
|||
Relationships
|
|||
| Is a |
autosomal recessive disease primary immunodeficiency disease |
||
| Part of | |||
|
Synonyms & Secondary IDs
|
|||
| Synonyms | |||
|
|
|||
| Secondary IDs | |||
|
|
|||
|
External Crossreferences & Linkouts
|
|||
|
GARD:6357 MESH:D004819 MIM:PS226400 NCI:C126877 ORDO:302 SNOMEDCT_US_2023_03_01:19138001 UMLS_CUI:C0014522 |
|||