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Metadata
ID	DOID:0080327
Name	multinucleated neurons, anhydramnios, renal dysplasia, cerebellar hypoplasia and hydranencephaly
Definition	A syndrome that is characterized by severe hydranencephaly with almost complete absence of the cerebral hemispheres, which are replaced by fluid, relative preservation of the posterior fossa structures, and renal dysplasia or agenesis and has_material_basis_in autosomal recessive homozygous mutation in the CEP55 gene on chromosome 10q23. https://www.ncbi.nlm.nih.gov/pubmed/?term=28264986
Xrefs	OMIM:236500
Synonyms	MARCH [EXACT]
Parent Relationships	is_a syndrome is_a autosomal recessive disease