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Summary Literature (0)
MIM:616900 - HYPOTONIA, INFANTILE, WITH PSYCHOMOTOR RETARDATION AND CHARACTERISTIC FACIES 3; IHPRF3

Xenbase Genes: tbck

Human Disease Resource: MIM

Mondo Disease Ontology (on Monarch Initiative):
MONDO:0014823 - hypotonia, infantile, with psychomotor retardation and characteristic facies 3