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Summary Literature (0)
MIM:615419 - HYPOTONIA, INFANTILE, WITH PSYCHOMOTOR RETARDATION AND CHARACTERISTIC FACIES 1; IHPRF1

Xenbase Genes: nalcn

Human Disease Resource: OMIM

Mondo Disease Ontology (on Monarch Initiative):
MONDO:0014176 - hypotonia, infantile, with psychomotor retardation and characteristic facies
MONDO:0024567 - hypotonia, infantile, with psychomotor retardation and characteristic facies 1