megalencephaly
A congenital abnormality in which the occipitofrontal circumference is greater than two standard deviations above the mean for a given age. It is associated with hydrocephalus; subdural effusion; arachnoid cysts; or is part of a genetic condition (e.g., alexander disease; sotos syndrome). [ MESH:D058627 ]
Term info
- Orphanet:2477 (MONDO:equivalentTo)
- MESH:D058627 (MONDO:equivalentTo)
- HP:0001355 (MONDO:otherHierarchy)
- SCTID:9740002 (MONDO:equivalentTo)
- MedDRA:10050183 (Orphanet:2477/e)
- ICD9:742.4 (MONDO:relatedTo)
ordo_malformation_syndrome
megalencephaly (disease)
http://identifiers.org/meddra/10050183
A congenital abnormality in which the occipitofrontal circumference is greater than two standard deviations above the mean for a given age. It is associated with hydrocephalus; subdural effusion; arachnoid cysts; or is part of a genetic condition (e.g., alexander disease; sotos syndrome).
http://purl.obolibrary.org/obo/Orphanet_2477, http://identifiers.org/mesh/D058627, http://identifiers.org/snomedct/9740002
megalencephaly (disease), macroencephaly, megalencephaly
MONDO:0016608