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MIM:617051 - NEURODEVELOPMENTAL DISORDER WITH MICROCEPHALY AND GRAY SCLERAE; NEDMIGS
Xenbase Genes: pus3
Human Disease Resource: MIM
MONDO:0014886 - distal epiphysis of distal phalanx of manual digit |
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MONDO:0014886 - distal epiphysis of distal phalanx of manual digit |