| Preferred Name |
Microgyria |
| ID |
http://ncicb.nci.nih.gov/xml/owl/EVS/Thesaurus.owl#C98988 |
| code |
C98988 |
| Concept_In_Subset | |
| Contributing_Source |
NICHD |
| DEFINITION |
A congenital abnormality characterized by the presence of abnormally small convolutions in the brain. It results in mental retardation. |
| Has_NICHD_Parent | |
| label |
Microgyria |
| NICHD_Hierarchy_Term |
Microgyria |
| Preferred_Name |
Microgyria |
| prefixIRI |
C98988 |
| prefLabel |
Microgyria |
| Semantic_Type |
Disease or Syndrome |
| UMLS_CUI |
C2362742 |
| subClassOf |
| Delete | Mapping To | Ontology | Source |
|---|---|---|---|
| http://purl.bioontology.org/ontology/OMIM/MTHU037257 | Online Mendelian Inheritance in Man | LOOM |