|
| General Information | |||
|---|---|---|---|
| Term | autosomal recessive congenital ichthyosis 7 | ID (Ontology) | DOID:0060716 (Human Disease) |
| Definition | An autosomal recessive congenital ichthyosis characterized by fine whitish scales, moderate to severe erythroderma, compact hyperkeratosis, hypergranulosis, acanthosis, and papillomatosis that has_material_basis_in variation in the chromosome region 12p11.2-q13.1. | ||
| Also Known As | "ARCI7" | ||
| 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 recessive disease__ physical disorder____________| ichthyosis___________________| autosomal recessive congenital ichthyosis |__autosomal recessive congenital ichthyosis 7 |
| Spanning Tree View Settings | |||
|---|---|---|---|
| Parents/Children View Depth |
|||
Relationships
|
|||
| Is a | autosomal recessive congenital ichthyosis | ||
| Part of | |||
|
Synonyms & Secondary IDs
|
|||
| Synonyms | |||
|
|||
| Secondary IDs | |||
|
|
|||
|
External Crossreferences & Linkouts
|
|||
|
ICD10CM:Q80.2 MIM:615022 |
|||