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MIM:615381 - MANDIBULAR HYPOPLASIA, DEAFNESS, PROGEROID FEATURES, AND LIPODYSTROPHY SYNDROME; MDPL
Xenbase Genes: pold1
Human Disease Resource: OMIM
MONDO:0014157 - mandibular hypoplasia-deafness-progeroid syndrome |
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MONDO:0014157 - mandibular hypoplasia-deafness-progeroid syndrome |