| General Information | |||
|---|---|---|---|
| Term | myelomeningocele | ID (Ontology) | DOID:0060326 (Human Disease) |
| Definition | A spina bifida characterized by protrusion of the spinal cord through an opening, covered by meningeal membranes. | ||
| 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
|
|||
|
||||||
neural tube defect |__spina bifida________________ central nervous system disease | |__spinal cord disease_________| myelomeningocele |
| Spanning Tree View Settings | |||
|---|---|---|---|
| Parents/Children View Depth |
|||
Relationships
|
|||
| Is a |
spina bifida spinal cord disease |
||
| Part of | |||
Synonyms & Secondary IDs
|
|||
| Synonyms | |||
|
|
|||
| Secondary IDs | |||
|
|
|||
External Crossreferences & Linkouts
|
|||
|
ICD10CM:Q05 MESH:D008591 NCI:C101201 NCI:C98874 SNOMEDCT_US_2023_03_01:268308005 SNOMEDCT_US_2023_03_01:7096005 UMLS_CUI:C0025312 UMLS_CUI:C0086664 UMLS_CUI:C0751316 |
|||