| General Information | |||
|---|---|---|---|
| Term | fibrochondrogenesis | ID (Ontology) | DOID:0060465 (Human Disease) |
| Definition | An osteochondrodysplasia that is characterized by shortened long bones in the arms and legs that are unusually wide at the ends, flattened vertebrae with a characteristic pinched or pear shape, and a very narrow chest in infants with short, wide ribs and a round and prominent abdomen. | ||
| 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
|
|||
|
||||||
bone development disease__ cartilage disease_________| osteochondrodysplasia |__fibrochondrogenesis 1 rec. |__fibrochondrogenesis 1 1 rec. |__fibrochondrogenesis 2 |
| Spanning Tree View Settings | |||
|---|---|---|---|
| Parents/Children View Depth |
|||
Relationships
|
|||
| Is a | osteochondrodysplasia | ||
| Part of | |||
Synonyms & Secondary IDs
|
|||
| Synonyms | |||
|
|
|||
| Secondary IDs | |||
|
|
|||
External Crossreferences & Linkouts
|
|||
|
GARD:2321 MESH:C562524 MIM:PS228520 ORDO:2021 SNOMEDCT_US_2023_03_01:17144009 UMLS_CUI:C0265282 |
|||