| General Information | |||
|---|---|---|---|
| Term | acrofacial dysostosis Rodriguez type | ID (Ontology) | DOID:0060383 (Human Disease) |
| Definition | An acrofacial dysostosis that is characterized by CNS malformations, lung anomalies, congenital heart defects, dysmorphic facies and limb reduction, and has_material_basis_in autosomal recessive inheritance. | ||
| Also Known As | "acrofacial dysostosis, syndrome of Rodriguez" | ||
| 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
|
|||
|
||||||
dysostosis |__acrofacial dysostosis |__acrofacial dysostosis Rodriguez type |
| Spanning Tree View Settings | |||
|---|---|---|---|
| Parents/Children View Depth |
|||
Relationships
|
|||
| Is a | acrofacial dysostosis | ||
| Part of | |||
Synonyms & Secondary IDs
|
|||
| Synonyms | |||
|
|||
| Secondary IDs | |||
|
|
|||
External Crossreferences & Linkouts
|
|||
|
GARD:496 MESH:C538183 MIM:201170 ORDO:1788 SNOMEDCT_US_2023_03_01:720430002 UMLS_CUI:C1860119 |
|||