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Disease Browser
Parent Node: Cerebellar Diseases (D002526)
Parent Node: Porencephaly (D065708)
..Starting node ..Porencephaly cerebellar hypoplasia malformations (C536336)
Child Nodes:
Sister Nodes:
..Porencephaly cerebellar hypoplasia malformations (C536336)
Human Disease MESH is developed by UMLS. Further data from MedGen, OMIM, CTD

Term ID:	9136
Name:	Porencephaly cerebellar hypoplasia malformations
Definition:
Alternative IDs:
ParentIDs:	MESH:D002526\|MESH:D065708
TreeNumbers:	C05.660.207.620.500/C536336 \|C10.228.140.252/C536336 \|C10.500.507.500.625/C536336 \|C16.131.621.207.620.500/C536336 \|C16.131.666.507.500.625/C536336
Synonyms:	Porencephaly, cerebellar hypoplasia, and internal malformations
Slim Mappings:	Congenital abnormality\|Musculoskeletal disease\|Nervous system disease
Reference:	MedGen: C536336 MeSH: C536336 OMIM: Genes:
Phenotypes
Disease Causing ClinVar Variants