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Summary Literature (0)
MIM:616801 - HYPOTONIA, INFANTILE, WITH PSYCHOMOTOR RETARDATION AND CHARACTERISTIC FACIES 2; IHPRF2

Xenbase Genes: unc80

Human Disease Resource: MIM

Mondo Disease Ontology (on Monarch Initiative):
MONDO:0014176 - hypotonia, infantile, with psychomotor retardation and characteristic facies
MONDO:0014777 - spinal neuromere