|
| General Information | |||
|---|---|---|---|
| Term | brachydactyly type A4 | ID (Ontology) | DOID:0110967 (Human Disease) |
| Definition | A brachydactyly characterized by autosomal dominant inheritance of hypoplastic middle phalanges, brachymesophalangy affecting mainly the 2nd and 5th digits and congenital talipes calcaneovalgus. | ||
| Also Known As | "BDA4" ; "brachymesophalangy II and V" ; "Temtamy type brachydactyly" | ||
| 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 |__brachydactyly |__brachydactyly type A4 |
| Spanning Tree View Settings | |||
|---|---|---|---|
| Parents/Children View Depth |
|||
Relationships
|
|||
| Is a | brachydactyly | ||
| Part of | |||
|
Synonyms & Secondary IDs
|
|||
| Synonyms | |||
|
|||
| Secondary IDs | |||
|
|
|||
|
External Crossreferences & Linkouts
|
|||
|
GARD:990 ICD10CM:Q73.8 MIM:112800 ORDO:93394 |
|||