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OMIM:613668 - MICROCEPHALY, POSTNATAL PROGRESSIVE, WITH SEIZURES AND BRAIN ATROPHY
Xenbase Genes: med17
Human Disease Resource: OMIM
MONDO:0013351 - infantile cerebral and cerebellar atrophy with postnatal progressive microcephaly |
DOID:0111262 - infantile cerebral and cerebellar atrophy with postnatal progressive microcephaly |