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 |