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MIM:618810 - PONTOCEREBELLAR HYPOPLASIA, HYPOTONIA, AND RESPIRATORY INSUFFICIENCY SYNDROME, NEONATAL LETHAL; PHRINL
Xenbase Genes:
Human Disease Resource: OMIM
MONDO:0032931 - pontocerebellar hypoplasia, hypotonia, and respiratory insufficiency syndrome, neonatal lethal |
DOID:0081396 - neonatal lethal pontocerebellar hypoplasia, hypotonia, and respiratory insufficiency syndrome |