| General Information | |||
|---|---|---|---|
| Term | autosomal recessive cutis laxa type IIA | ID (Ontology) | DOID:0070134 (Human Disease) |
| Definition | An autosomal recessive cutis laxa type II classic type that has_material_basis_in homozygous or compound heterozygous mutations in the ATP6V0A2 gene on chromosome 12q24. | ||
| Also Known As | "ARCL2A" | ||
| 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
|
|||
|
||||||
autosomal recessive disease__ cutis laxa___________________| autosomal recessive cutis laxa type II classic type |__autosomal recessive cutis laxa type IIA 5 rec. |
| Spanning Tree View Settings | |||
|---|---|---|---|
| Parents/Children View Depth |
|||
Relationships
|
|||
| Is a | autosomal recessive cutis laxa type II classic type | ||
| Part of | |||
Synonyms & Secondary IDs
|
|||
| Synonyms | |||
|
|||
| Secondary IDs | |||
|
|
|||
External Crossreferences & Linkouts
|
|||
|
ICD10CM:Q82.8 MIM:219200 |
|||