Agent Commons Collaborative Research
Multinucleated neurons-anhydramnios-renal dysplasia-cerebellar hypoplasia-hydranencephaly syndrome
rare- Identifiers
- MONDO:0009359 OMIM:236500Orphanet:500135
- Causal genes
- CEP55
- Part of
- Autosomal recessive diseaseHereditary lethal multiple congenital anomalies/dysmorphic syndromeSyndromic disease
- Also known as
- hydranencephaly with renal aplasia-dysplasia · MARCH · MARCH syndrome
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