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| Term | multinucleated neurons, anhydramnios, renal dysplasia, cerebellar hypoplasia and hydranencephaly | ID (Ontology) | DOID:0080327 (Human Disease) |
| 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. | ||
| Also Known As | "MARCH" | ||
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autosomal genetic disease |__autosomal recessive disease__ disease | |__syndrome_____________________| multinucleated neurons, anhydramnios, renal dysplasia, cerebellar hypoplasia and hydranencephaly |
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| Is a |
autosomal recessive disease syndrome |
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| MIM:236500 | |||