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Summary Literature (0)
OMIM:613668 - MICROCEPHALY, POSTNATAL PROGRESSIVE, WITH SEIZURES AND BRAIN ATROPHY

Xenbase Genes: med17

Human Disease Resource: OMIM

Mondo Disease Ontology (on Monarch Initiative):
MONDO:0013351 - infantile cerebral and cerebellar atrophy with postnatal progressive microcephaly

Disease Ontology (DO):
DOID:0111262 - infantile cerebral and cerebellar atrophy with postnatal progressive microcephaly